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Journal articles on the topic 'Tert-Butylbenzene'

Author: Grafiati

Published: 4 June 2021

Last updated: 28 July 2025

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1

Chirico, Robert D., and William V. Steele. "Thermodynamic properties of tert-butylbenzene and 1,4-di-tert-butylbenzene." Journal of Chemical Thermodynamics 41, no. 3 (2009): 392–401. http://dx.doi.org/10.1016/j.jct.2008.10.008.

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2

de Koning, A. J. "Preparation of some derivatives of meta-di-tert-butylbenzene and tert-butylbenzene." Recueil des Travaux Chimiques des Pays-Bas 92, no. 8 (2010): 839–44. http://dx.doi.org/10.1002/recl.19730920805.

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3

Shernyukov, Andrey V., Alexander M. Genaev, George E. Salnikov, Vyacheslav G. Shubin, and Henry S. Rzepa. "Elevated reaction order of 1,3,5-tri-tert-butylbenzene bromination as evidence of a clustered polybromide transition state: a combined kinetic and computational study." Organic & Biomolecular Chemistry 17, no. 15 (2019): 3781–89. http://dx.doi.org/10.1039/c9ob00607a.

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The kinetics and mechanism of concurrent bromo-de-protonation and bromo-de-tert-butylation of 1,3,5-tri-tert-butylbenzene at different bromine concentrations were studied experimentally and theoretically.

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4

Shimizu, Tomoe, Katsuhiro Hita, Arjun Paudel, Junnji Tanaka, and Takehiko Yamato. "Synthesis of polymethyl substituted [2.2]metaparacyclophanes and their Lewis-acid induced isomerisation to [2.2]metacyclophanes." Journal of Chemical Research 2009, no. 4 (2009): 244–47. http://dx.doi.org/10.3184/030823409x430185.

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The preparation of polymethyl substituted [2.2]metaparacyclophanes using sulfur method and the X-ray structure determination of 4,5,6,8,12,13,15,16-octamethyl[2.2]metaparacyclophane are described. AlCl3-MeNO2-catalysed trans- tert-butylation of 5- tert-butyl-8,12,13,15,16-pentamethyl[2.2]metaparacyclophane in benzene led to isomerisation reaction to afford the strainless 8,12,13,14,16-pentamethyl[2.2]metacyclophane in 85% yield along with tert-butylbenzene.

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5

Shimizu, Tomoe, Katsuhiko Hida, and Takehiko Yamato. "Synthesis of 5-tert-butyl-8,12,14-trimethyl- and 5-tert-butyl-8,12,14,16-tetramethyl[2.2]metacyclophane and their treatment with Lewis acids in benzene." Journal of Chemical Research 2009, no. 7 (2009): 443–47. http://dx.doi.org/10.3184/030823409x465222.

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Treatment of 5- tert-butyl-8,12,14,16-tetramethyl[2.2]MCP with AlCl3-MeNO2 in benzene led to trans- tert-butylation to afford 8,12,14,16-tetramethyl[2.2]MCP in good yield along with tert-butylbenzene. On the other hand, the same treatment of 5- tert-butyl-8,12,14-trimethyl[2.2]MCP led to transannular cyclisation reaction and isomerisation reaction to afford the corresponding strainless 2- tert-butyl-3a,6,8-trimethyl-3,3a,4,5,9,10-hexahydropyrene in good yield.

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6

Drath, Olga, Robert W. Gable, and Colette Boskovic. "Structural investigation of one- and two-dimensional coordination polymers based on cobalt–bis(dioxolene) units and 1-hydroxy-1,2,4,5-tetrakis(pyridin-4-yl)cyclohexane." Acta Crystallographica Section C Structural Chemistry 74, no. 6 (2018): 734–41. http://dx.doi.org/10.1107/s205322961800671x.

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The combination of cobalt, 3,5-di-tert-butyldioxolene (3,5-dbdiox) and 1-hydroxy-1,2,4,5-tetrakis(pyridin-4-yl)cyclohexane (tpch) yields two coordination polymers with different connectivities, i.e. a one-dimensional zigzag chain and a two-dimensional sheet. Poly[[bis(3,5-di-tert-butylbenzene-1,2-diolato)bis(1,5-di-tert-butyl-4-oxocyclohexa-2,5-dien-1-yl-3-olato)[μ4-1-hydroxy-1,2,4,5-tetrakis(pyridin-4-yl)cyclohexane]cobalt(III)]–ethanol–water 1/7/5], {[Co2(C14H20O2)4(C26H24N4O)]·7C2H5OH·5H2O} n or {[Co2(3,5-dbdiox)4(tpch)}·7EtOH·5H2O} n , is the second structurally characterized example of a

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7

Xu, Xiao-Bin, Fei-Fei Lan, Shi-Yao Yang, Rong-Bin Huang, and Seik Weng Ng. "5-tert-Butylbenzene-1,3-dicarboxylic acid." Acta Crystallographica Section E Structure Reports Online 63, no. 9 (2007): o3747. http://dx.doi.org/10.1107/s1600536807038408.

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8

Wang, Guo-wei, Wen-yuan Wu, Ling-hua Zhuang, and Jin-tang Wang. "1,4-Bis(benzyloxy)-2-tert-butylbenzene." Acta Crystallographica Section E Structure Reports Online 64, no. 3 (2008): o620. http://dx.doi.org/10.1107/s1600536808003383.

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9

van Hartingsveldt, W., P. E. Verkade, and B. M. Wepster. "Synthesis of 1,3,5-tri-tert. Butylbenzene." Recueil des Travaux Chimiques des Pays-Bas 75, no. 3 (2010): 349–54. http://dx.doi.org/10.1002/recl.19560750314.

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10

Wang, Xia, Jun-long Niu, and Cai-xia Zhi. "2,4-Dibromo-6-tert-butylbenzene-1,3-diol." Acta Crystallographica Section E Structure Reports Online 67, no. 10 (2011): o2618. http://dx.doi.org/10.1107/s1600536811034866.

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11

Chirico, Robert D., and William V. Steele. "Corrigendum to ‘‘Thermodynamic properties of tert-butylbenzene and 1,4-di-tert-butylbenzene [J. Chem. Thermodyn. 41 (2009) 392–401]”." Journal of Chemical Thermodynamics 41, no. 10 (2009): 1186. http://dx.doi.org/10.1016/j.jct.2009.03.013.

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12

Faulk, James D., and Robert C. Dunbar. "Time-resolved photodissociation of three tert-butylbenzene ions." Journal of Physical Chemistry 95, no. 18 (1991): 6932–36. http://dx.doi.org/10.1021/j100171a037.

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13

Saïd, Anes El-Hadj, and Sidi Mohamed Mekelleche. "Investigation of Reaction Mechanisms and Kinetics of the Radical Scavenging Ability of 5-Tert-Butylbenzene-1,2,3-Triol and 3,5-di-Tert-Butylbenzene-1,2-Diol Compounds Towards OOH Radical." Progress in Reaction Kinetics and Mechanism 43, no. 2 (2018): 101–11. http://dx.doi.org/10.3184/146867818x15161889114484.

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The antioxidant properties of the synthesised 5- tert-butylbenzene-1,2,3-triol (system A) and the designed 3,5-di -tert-butylbenzene-1,2-diol (system B) have been explored through density functional theory at the M05-2X/6-31+G(d,p) level of theory. The quantum mechanics-based test for overall free radical scavenging activity (QM- ORSA) protocol has been employed to account for their radical-scavenging capacity against the hydroperoxyl radical (HOO•) in the gas phase and in toluene solvent as a mimic lipid medium. The different mechanisms of the chemical reactions of the studied systems with HO

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14

Zdarta, Agata, Amanda Pacholak, Marta Galikowska, Wojciech Smułek, and Ewa Kaczorek. "Butylbenzene and tert-Butylbenzene—Sorption on Sand Particles and Biodegradation in the Presence of Plant Natural Surfactants." Toxins 10, no. 9 (2018): 338. http://dx.doi.org/10.3390/toxins10090338.

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The effects of hydrocarbons sorption on sand and saponins presence in the system on butylbenzene and tert-butylbenzene biological degradation was investigated. Additionally, the impact of saponins-containing plant extracts on environmental microorganisms was studied. Results of cell surface property measurements in samples with saponins only revealed changes in cell surface hydrophobicity, electrokinetic potential and membrane permeability when compared to corresponding values for glucose-grown microbes. Subsequently, in sorption experiments, the hydrocarbon adsorption kinetics in bacteria-fre

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15

Noh, Kyungkyou, та Jaheon Kim. "Poly[(μ3-5-tert-butylbenzene-1,3-dicarboxylato)dipyridinecobalt(II)]". Acta Crystallographica Section E Structure Reports Online 69, № 11 (2013): m579—m580. http://dx.doi.org/10.1107/s1600536813026640.

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In the title compound, [Co(C12H12O4)(C5H5N)2]n, the CoIIcation is coordinated by four O atoms from three 5-tert-butylbenzene-1,3-dicarboxylate anions and two N atoms from pyridine molecules in a distorted octahedral geometry. One carboxylate group of the anionic ligand chelates a CoIIcation while another carboxylate group bridges two CoIIcations, resulting in a polymeric layer parallel to (101). Weak C—H...O hydrogen bonds occur between adjacent polymeric layers. In the crystal, one of pyridine molecules is equally disordered over two positions.

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16

Kasperczyk, Kornela, Beata Orlińska, and Jan Zawadiak. "Aerobic oxidation of cumene catalysed by 4-alkyloxycarbonyl-N-hydroxyphthalimide." Open Chemistry 12, no. 11 (2014): 1176–82. http://dx.doi.org/10.2478/s11532-014-0565-8.

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Abstract4-Hexyloxycarbonyl-, 4-dodecyloxycarbonyl- and 4-hexadecyloxycarbonyl-N-hydroxyphthalimides were synthesised using trimellitic anhydride chloride as the starting material. The obtained lipophilic derivatives of N-hydroxyphthalimide were applied as catalysts of the cumene oxidation reaction with oxygen performed in polar acetonitrile, in non-polar tert-butylbenzene and in the absence of a solvent. The courses of reactions catalysed by N-hydroxyphthalimide and its derivatives were compared.

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17

Wang, Lin, Jiahao Jing, Chao Zhang, Yanhong Ouyang, Dingwei Sun, and Huazhi Wu. "Treatment activity of hydrogels loaded with cobalt metal–organic frameworks of urinastatin on sepsis acute lung injury." Materials Express 13, no. 3 (2023): 536–41. http://dx.doi.org/10.1166/mex.2023.2376.

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The reaction of Co(II) salt with 5-tert-butylbenzene-1,3-dicarboxylic acid (5-tert-H2IPA) and N,N′-bis(3-pyridyl) terephthalamide (L) in a mixed solvent of H2O and CH3CN affords a new coordination polymer [Co(L)0.5(5-tert-IPA)]n (1). Based on the slow release of the drug, hydrogels loaded with Co(II) metal–organic frameworks of urinastatin were prepared. SEM images showed that the hydrogels had a highly porous morphology. Furthermore, the treatment activity of the hydrogels on sepsis acute lung injury was assessed. ELISA detection results showed that the hydrogels significantly reduced the lev

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18

Weniger, K., J. Kleimann, and H. Fr Grützmacher. "Mass spectrometry of tert-butylnaphthalenes–a comparison with the unimolecular fragmentation of tert-butylbenzene." European Journal of Mass Spectrometry 3, no. 1 (1997): 271. http://dx.doi.org/10.1255/ejms.23.

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19

Keypour, Hassan, Ahmad Ali Dehghani-Firouzabadi, Maryam Shayesteh, and Sadegh Salehzadeh. "Synthesis and Characterisation of Macrocyclic Copper(II) Complexes Containing N3O4 Donor Sets." Journal of Chemical Research 2008, no. 10 (2008): 587–88. http://dx.doi.org/10.3184/030823408x360184.

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Two new macrocyclic Schiff-base complexes of Cu(II) have been prepared by the template reaction of 2,6-bis (2-formylphenoxymethyl)pyridine with 1,2-bis(2′-aminophenoxy)benzene [L1] or with 1,2-bis(2′-aminophenoxy)-4-tert-butylbenzene [L2] in the presence of Cu(II) perchlorate. The amines used have low flexibility and therefore the formation of complexes was very difficult. The synthesised 23-membered, heptadentate N3O4 complexes were characterised by elemental analysis, IR, and FAB-mass spectroscopy.

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20

Wei, Xiao-Meng, Shan-Shan Guo, Hua Yan, Xian-Long Cheng, Feng Wei, and Shu-Shan Du. "Contact Toxicity and Repellency of the Essential Oil from Bupleurum bicaule Helm against Two Stored Product Insects." Journal of Chemistry 2018 (2018): 1–8. http://dx.doi.org/10.1155/2018/5830864.

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Essential oils obtained from many plants showed various kinds of insecticidal properties; some of them have been considered as alternative insecticides for pest control. The present study was aimed at determining the chemical composition of the essential oil from the roots of Bupleurum bicaule Helm, as well as evaluating the contact and repellent activities of the oil and four identified compounds against Lasioderma serricorne and Liposcelis bostrychophila adults. The essential oil was extracted by hydrodistillation, and its components were analyzed by gas chromatography-mass spectrometry (GC-

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21

Ederer, H. J., A. Kruse, C. Mas, and K. H. Ebert. "Modelling of the pyrolysis of tert-butylbenzene in supercritical water." Journal of Supercritical Fluids 15, no. 3 (1999): 191–204. http://dx.doi.org/10.1016/s0896-8446(99)00013-3.

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22

Ho, Yen Peng, and Robert C. Dunbar. "Cooling of tri-tert-butylbenzene ions: a TRPD thermometric study." Journal of Physical Chemistry 97, no. 44 (1993): 11474–79. http://dx.doi.org/10.1021/j100146a021.

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23

Kruse, Andrea, and K. H. Ebert. "Chemical Reactions in Supercritical Water - 1. Pyrolysis of tert.-Butylbenzene." Berichte der Bunsengesellschaft für physikalische Chemie 100, no. 1 (1996): 80–83. http://dx.doi.org/10.1002/bbpc.19961000115.

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24

FAULK, J. D., and R. C. DUNBAR. "ChemInform Abstract: Time-Resolved Photodissociation of Three tert.-Butylbenzene Ions." ChemInform 22, no. 49 (2010): no. http://dx.doi.org/10.1002/chin.199149038.

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25

Knoester, C. J., A. J. de Koning, P. E. Verkade, and B. M. Wepster. "Preparation of some new derivatives of meta-di-tert-butylbenzene." Recueil des Travaux Chimiques des Pays-Bas 86, no. 1 (2010): 5–14. http://dx.doi.org/10.1002/recl.19670860102.

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26

Palijczuk, D., V. M. Gun'ko, R. Leboda, J. Skubiszewska-Zięba, and S. Ziętek. "Porous Structure of Activated Carbons and Tert-butylbenzene Breakthrough Dynamics." Journal of Colloid and Interface Science 250, no. 1 (2002): 5–17. http://dx.doi.org/10.1006/jcis.2002.8318.

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27

Kantlehner, Willi, Erwin Haug, Oliver Scherr, and Georg Ziegler. "Orthoamide, LIX. Formyl-aalen [Tris(diformylamino)methan] – ein neues Formylierungsmittel für aktivierte Aromaten/Orthoamides, LIX. Formyl-aalen [Tris(diformylamino)methane] – a New Formylating Reagent for Activated Aromatic Compounds." Zeitschrift für Naturforschung B 57, no. 11 (2002): 1295–304. http://dx.doi.org/10.1515/znb-2002-1116.

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In the presence of strong Lewis acids such as aluminum chloride or boron trichloride, formyl-aalen [tris(diformylamino)methane] (3) acts as a formylating reagent for aromatic alkane compounds and aromatic ethers. The orthoamide 3 delivers three formyl groups for the formylation process. Thus toluene, cumene, tert-butylbenzene, hexylbenzene, ο-xylene, ρ-cymene, biphenyl, anisole, diphenylether and 1,3-dimethoxybenzene can be formylated in 1,2-dichloroethane. In these reactions, 3 and aluminum chloride should be used in a molar ratio of 1:6 to 1:9.

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28

Schaefer, Ted, Rudy Sebastian, Glenn H. Penner, and S. R. Salman. "The proximate spin–spin coupling, 5J(F,CH3), as a quantitative conformational indicator in alkylfluorobenzenes and related compounds." Canadian Journal of Chemistry 64, no. 8 (1986): 1602–6. http://dx.doi.org/10.1139/v86-266.

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The through-space or proximate nuclear spin–spin coupling constant, 5J(F,CH3) = 5J, between methyl protons and ring fluorine nuclei in alkylfluorobenzenes is postulated as [Formula: see text] θ being the torsional angle for the [Formula: see text] bond. A and B are obtained from the known internal rotational behaviour in 2,6-difluoroethylbenzene and the corresponding cumene derivative. The parameterization is tested on the observed 5J in derivatives of 2,4,6-tri-tert-butyl- and 2,4,6-tri-isopropyl-fluorobenzene, in 2-chloro-6-fluoroisopropylbenzene, 2,6-difluoro-α-methylstyrene, and N-methyl-8

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29

Komen, Corine M. D., and Friedrich Bickelhaupt. "Easy Preparation of 1,3-Di-tert-Butylbenzene and Some Derivatives Thereof." Synthetic Communications 26, no. 9 (1996): 1693–97. http://dx.doi.org/10.1080/00397919608002608.

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30

Dilek, Cerag, Charles W. Manke, and Esin Gulari. "Phase behavior of 1,3,5-tri-tert-butylbenzene–carbon dioxide binary system." Journal of Supercritical Fluids 43, no. 3 (2008): 421–29. http://dx.doi.org/10.1016/j.supflu.2007.07.009.

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31

Guzei, I. A., C. E. Reck, and C. H. Winter. "Crystal structure of l,4-diiodo-2,5-di-tert-butylbenzene, C14H20I2." Zeitschrift für Kristallographie - New Crystal Structures 213, no. 1-4 (1998): 223–24. http://dx.doi.org/10.1524/ncrs.1998.213.14.223.

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32

FRY, A. J., and S. SOLOMON. "ChemInform Abstract: 2,4-Di-tert-butylbromobenzene by Silver Ion-Assisted Bromination of 1,3-Di-tert-butylbenzene." ChemInform 23, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199206142.

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33

Marczewski, Marek, Magdalena Kominiak, Magdalena Dul, and Hanna Marczewska. "The role of butylbenzene carbenium ions in the acid catalyzed cracking of polystyrene. Transformation of n-butylbenzene, sec-butylbenzene, iso-butylbenzene, tert-butylbenzene, 4-phenyl-1-butene, n-propylbenzene and n-hexylbenzene over silicaalumina and alumina acid catalysts." Reaction Kinetics, Mechanisms and Catalysis 119, no. 1 (2016): 107–20. http://dx.doi.org/10.1007/s11144-016-1050-5.

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34

Nakayama, Juzo, Shoji Yamaoka, Tomoko Nakanishi, and Masamatsu Hoshino. "3,4-Di-tert-butylthiophene 1,1-dioxide, a convenient precursor of o-Di-tert-butylbenzene and its derivatives." Journal of the American Chemical Society 110, no. 19 (1988): 6598–99. http://dx.doi.org/10.1021/ja00227a069.

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35

Sudha, S., M. Palanichamy, V. V. Balasubramanian, Banumathi Arabindoo, and V. Murugesan. "The vapour phase reaction of tert-butylbenzene and tert-butyl acetate over Al-MCM-41 molecular sieves." Journal of Molecular Catalysis A: Chemical 255, no. 1-2 (2006): 220–29. http://dx.doi.org/10.1016/j.molcata.2006.03.050.

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36

Huszthy, Péter, Mária Kajtár-Peredy, Károly Lempert, and Judit Hegedüs-Vajda. "The reaction of triphenylmethyl halides with triphenylphosphine in cumene and tert-butylbenzene." J. Chem. Soc., Perkin Trans. 2, no. 3 (1992): 347–53. http://dx.doi.org/10.1039/p29920000347.

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37

Khasanshin, Talgat S., Vladimir S. Samuilov, Alexander P. Shchamialiou, Dana Drăgoescu, and Florinela Sîrbu. "Thermodynamic properties of cumene, tert-butylbenzene, and n-hexadecane under elevated pressures." Journal of Chemical Thermodynamics 134 (July 2019): 96–105. http://dx.doi.org/10.1016/j.jct.2019.03.005.

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38

Srinivasan, Sekar, and Ravi Divahar. "An Analysis of the Effects of Volatile Organic Compound (Odour Emissions) from Municipal Solid Waste Dumps on the Environment and Quality of Life." Current World Environment 20, no. 1 (2025): 182–94. https://doi.org/10.12944/cwe.20.1.14.

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The public is severely concerned about the odours rising from municipal solid waste dumping yards (MSWDYs). In this study, odour emissions from MSWDYs were assessed at fresh wastes, as well as over a summer season, in semi urban area of Thiruporur, Chennai. Samples were collected with a BDX II abatement air sampler and an ADT probe and were analysed using GC-MS. During the disposal of fresh waste, among three stations around 18 different compounds with different concentration levels are identified. The maximum concentration of VOCs was recorded for tert-butylbenzene at 1.41 ?g/m3, while the lo

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39

Chen, Chia-Jou, Chia-Ling Chen, Yu-Hsiang Liu, et al. "Coordination Polymers Constructed from Semi-Rigid N,N′-Bis(3-pyridyl)terephthalamide and Dicarboxylic Acids: Effect of Ligand Isomerism, Flexibility, and Identity." Chemistry 3, no. 1 (2020): 1–12. http://dx.doi.org/10.3390/chemistry3010001.

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Reactions of the semi-rigid N,N′-bis(3-pyridyl)terephthalamide (L) with divalent metal salts in the presence of dicarboxylic acids afforded [Cd(L)0.5(1,2-BDC)(H2O)]n (1,2-H2BDC = benzene-1,2-dicarboxylic acid), 1, {[Cd(L)1.5(1,3-BDC)(H2O)]·5H2O}n (1,3-H2BDC = benzene-1,3-dicarboxylic acid), 2a, {[Cd(1,3-BDC)(H2O)3]·2H2O}n, 2b, {[Cd(L)0.5(1,4-BDC)(H2O)2]·H2O}n (1,4-H2BDC = benzene-1,4-dicarboxylic acid), 3, and [Cu(L)0.5(5-tert-IPA)]n (5-tert-IPA = 5-tert-butylbenzene-1,3-dicarboxylic acid), 4, which have been structurally characterized by single crystal X-ray diffraction. Complexes 1 and 3 are

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40

Petryk, Michael W. P., and Bryan R. Henry. "CH Stretching Vibrational Overtone Spectra oftert-Butylbenzene,tert-Butyl Chloride, andtert-Butyl Iodide." Journal of Physical Chemistry A 109, no. 18 (2005): 4081–91. http://dx.doi.org/10.1021/jp040710h.

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41

Ochiai, Masahito, Kunio Oxhima, Takao Ito, Yuko Masaki, and Motoo Shiro. "Synthesis and structure of 1-(diacetoxyiodo)-2,4,6-tri-tert-butylbenzene and its analogues." Tetrahedron Letters 32, no. 10 (1991): 1327–28. http://dx.doi.org/10.1016/s0040-4039(00)79658-4.

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42

Klingele, Marco H., and Berthold Kersting. "Notizen: Efficient Medium-Scale Synthesis of 2-Bromo-5-tert-butylbenzene-1,3-dicarbaldehyde." Zeitschrift für Naturforschung B 56, no. 4-5 (2001): 437–39. http://dx.doi.org/10.1515/znb-2001-4-519.

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Abstract A short and efficient multi-gram synthesis of the title compound has been designed which allows its preparation from commercially available material in only three steps in overall yields of 60-70 % .

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43

KOMEN, C. M. D., and F. BICKELHAUPT. "ChemInform Abstract: Easy Preparation of 1,3-Di-tert-butylbenzene and Some Derivatives Thereof." ChemInform 27, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.199633190.

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44

de Koning, Adrianus Jan. "Derivatives of meta-di-tert-butylbenzene. Part III: Preparation of some chlorinated derivatives." Recueil des Travaux Chimiques des Pays-Bas 95, no. 7-8 (2010): 160–62. http://dx.doi.org/10.1002/recl.19760950703.

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45

Burgers, J., W. van Hartingsveldt, J. van Keulen, P. E. Verkade, H. Visser, and B. M. Wepster. "Preparation and constitution of a number of derivatives of Meta-di-Tert. butylbenzene." Recueil des Travaux Chimiques des Pays-Bas 75, no. 11 (2010): 1327–42. http://dx.doi.org/10.1002/recl.19560751114.

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Liaw, Der-Jang, and Been-Yang Liaw. "Synthesis and Properties of Polyimides Derived from 1,4-Bis(4-aminophenoxy)-2-tert-butylbenzene." Polymer Journal 28, no. 11 (1996): 970–75. http://dx.doi.org/10.1295/polymj.28.970.

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Cho, Yoon Sung, Joong Chul Choe, and Myung Soo Kim. "Non-Rice-Ramsperger-Kassel-Marcus-Quasi-Equilibrium Theory Dissociation of tert-Butylbenzene Molecular Ion." Journal of Physical Chemistry 99, no. 21 (1995): 8645–51. http://dx.doi.org/10.1021/j100021a032.

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Klingele, Marco H., and Berthold Kersting. "ChemInform Abstract: Efficient Medium-Scale Synthesis of 2-Bromo-5-tert-butylbenzene-1,3-dicarbaldehyde." ChemInform 32, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.200136087.

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de Koning, Adrianus Jan. "Derivatives of m-di-tert-butylbenzene. Part VI. The preparation of miscellaneous halogenated compounds." Recueil des Travaux Chimiques des Pays-Bas 100, no. 11 (2010): 421–25. http://dx.doi.org/10.1002/recl.19811001108.

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Sathiyaraj, Manickam, and Perumal Venkatesh. "Synthesis of 1-butoxy-4-tert-butylbenzene under The Effect of Multi-site Phase Transfer Catalysis System – A Kinetic Study." Bulletin of Chemical Reaction Engineering & Catalysis 15, no. 2 (2020): 405–14. http://dx.doi.org/10.9767/bcrec.15.2.7519.405-414.

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Abstract:

Phase transfer catalysis technique proved to be a useful method for synthesizing various organic compounds under heterogeneous reactions and recognized as a viable environmentally friendly. The influence of a new multi site phase transfer catalyst (MPTC) is the synthesis of 1-butoxy-4-tertbutylbenzene from 4-tert-butylphenol with 1-bromobutane (BB) under heterogeneous solid-liquid condition using potassium hydroxide as a base at 60 °C. The higher conversion of 1-bromobutane was achieved by using the synergistic condition of multi-site phase transfer catalyst in better efficacy. The reaction ra

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