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Journal articles on the topic '2-Chlorobenzonitrile'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

B., Hari Babu, Venkateswara Rao K. T., Suh Y. W., Sai Prasad P. S., and Lingaiah N. "One-step selective synthesis of 2-chlorobenzonitrile from 2-chlorotoluene via ammoxidation." New Journal of Chemistry 42, no. 3 (2018): 1892–901. http://dx.doi.org/10.1039/c7nj03728g.

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Isolated and polymeric vanadia formulate V<sub>2</sub>O<sub>5</sub>/Al<sub>2</sub>O<sub>3</sub> catalysts selective for the synthesis of 2-chlorobenzonitrile from 2-chlorotoluene in a single step through ammoxidation.

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2

Onda, Masao, Masahiro Sakuma, Tatsuji Shimoe, Noriyuki Saegusa, and Ichiro Yamaguchi. "Microwave spectrum and quadrupole coupling constant of 2-chlorobenzonitrile." Journal of Molecular Structure 323 (July 1994): 287–88. http://dx.doi.org/10.1016/0022-2860(94)08311-8.

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3

Aim, Karel. "A modified ebulliometric method for high-boiling substances: vapour pressures of 2-chlorobenzonitrile and 4-chlorobenzonitrile at temperatures from 380 K to 490 K." Journal of Chemical Thermodynamics 26, no. 9 (1994): 977–86. http://dx.doi.org/10.1006/jcht.1994.1115.

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4

Trivedi, Mahendra Kumar, Alice Branton, Dahryn Trivedi, Gopal Nayak, Ragini Singh, and Snehasis Jana. "Experimental Investigation on Physical, Thermal and Spectroscopic Properties of 2-Chlorobenzonitrile: Impact of Biofield Treatment." Modern Chemistry 3, no. 4 (2015): 38–46. https://doi.org/10.5281/zenodo.35219.

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2-chlorobenzonitrile (2-ClBN) is widely used in the manufacturing of azo dyes, pharmaceuticals, and as intermediate in various chemical reactions. The aim of present study was to evaluate the impact of biofield treatment on physical, thermal and spectroscopic properties of 2-ClBN. 2-ClBN sample was divided into two groups that served as treated and control. The treated group received Mr. Trivedi’s biofield treatment. Subsequently, the control and treated samples were evaluated using X-ray diffraction (XRD), surface area analyser, differential scanning calorimetry (DSC), thermogravimetric

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5

Trivedi, Mahendra Kumar, Alice Branton, Dahryn Trivedi, Gopal Nayak, Ragini Singh, and Snehasis Jana. "Experimental Investigation on Physical, Thermal and Spectroscopic Properties of 2-Chlorobenzonitrile: Impact of Biofield Treatment." Modern Chemistry 3, no. 4 (2015): 38–46. https://doi.org/10.5281/zenodo.186726.

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2-chlorobenzonitrile (2-ClBN) is widely used in the manufacturing of azo dyes, pharmaceuticals, and as intermediate in various chemical reactions. The aim of present study was to evaluate the impact of biofield treatment on physical, thermal and spectroscopic properties of 2-ClBN. 2-ClBN sample was divided into two groups that served as treated and control. The treated group received Mr. Trivedi’s biofield treatment. Subsequently, the control and treated samples were evaluated using X-ray diffraction (XRD), surface area analyser, differential scanning calorimetry (DSC), thermogravimetric

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6

Buronov, A., A. Nasrullaev, Kh Bozorov, N. Lifei, and H. A. Aisa. "NEW TETRACYCLIC THIENO[3,2-d]PYRIMIDINE SCAFFOLD DERIVATIVES SYNTHESIZED AND AMINATED." 2022-yil 3-son (133/1) ANIQ FANLAR SERIYASI 1, no. 1 (2025): 12–17. https://doi.org/10.59251/2181-1296.2025.v1.149.2.3208.

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The synthesis of novel thieno[3,2-d]pyrimidine derivatives started with the reaction of 5-bromo-2 chlorobenzonitrile with ethyl-2-mercaptoacetate to give the compound AT-2. The addition of lactames to the formed AT-2 followed by cyclization gave the compound AR-05. The amination reaction was then used to facilitate the formation of a C-C bond. The intermediate AR-05 was formed under a base in dioxane in the presence of aromatic amines and a palladium catalyst, forming a new nitrogen-carbon bond. AR-58-1 and AR-82 were synthesized as end products. The structure of the new compounds was studied

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7

Buronov, A., A. Nasrullaev, Kh Bozorov, N. Lifei, S. Kulmirzaeva, and A. Ishankulov. "SYNTHESIS OF NOVEL TETRACYCLIC THIENO[3,2-d]PYRIMIDINONES." 2022-yil 3-son (133/1) ANIQ FANLAR SERIYASI 1, no. 1 (2025): 5–11. https://doi.org/10.59251/2181-1296.2025.v1.149.2.3206.

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The synthesis of novel thieno[3,2-d]pyrimidine derivatives commenced with 5-bromo-2-chlorobenzonitrile with ethyl-2-mercaptoacetate, which yielded the compound AT-2. The addition of piperidin-2-one to the formed AT-2 and subsequent cyclization yielded the compound AR-05. Subsequently, the Suzuki cross-coupling reaction was employed to facilitate the formation of a carbon-carbon bond. The intermediate AR-05 was formed in an alkaline medium in a toluene/water mixture in the presence of arylboronic acid and a palladium catalyst, forming a new C-C bond. AR-27 was synthesized as the final product.

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8

Mahendra, Kumar Trivedi, Branton Alice, Nayak Gopal, and Trivedi Dahryn. "Experimental Investigation on Physical, Thermal and Spectroscopic Properties of 2-Chlorobenzonitrile: Impact of Biofield Treatment." Modern Chemistry 3, no. 4 (2015): 38–46. https://doi.org/10.11648/j.mc.20150304.11.

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2-chlorobenzonitrile (2-ClBN) is widely used in the manufacturing of azo dyes, pharmaceuticals, and as intermediate in various chemical reactions. The aim of present study was to evaluate the impact of biofield treatment on physical, thermal and spectroscopic properties of 2-ClBN. 2-ClBN sample was divided into two groups that served as treated and control. The treated group received Mr. Trivedi’s biofield treatment. Subsequently, the control and treated samples were evaluated using X-ray diffraction (XRD), surface area analyser, differential scanning calorimetry (DSC), thermogravimetric

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9

Kumar Trivedi, Mahendra. "Experimental Investigation on Physical, Thermal and Spectroscopic Properties of 2-Chlorobenzonitrile: Impact of Biofield Treatment." Modern Chemistry 3, no. 4 (2015): 38. http://dx.doi.org/10.11648/j.mc.20150304.11.

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10

Sudha, S., N. Sundaraganesan, M. Kurt, M. Cinar, and M. Karabacak. "FT-IR and FT-Raman spectra, vibrational assignments, NBO analysis and DFT calculations of 2-amino-4-chlorobenzonitrile." Journal of Molecular Structure 985, no. 2-3 (2011): 148–56. http://dx.doi.org/10.1016/j.molstruc.2010.10.035.

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11

Geppert, W. D., N. Getoff, K. Sehested, and J. Holcman. "One electron reduction and oxidation of 2-, 3- and 4-chlorobenzonitrile in aqueous solution: a pulse radiolysis study." Radiation Physics and Chemistry 59, no. 1 (2000): 39–47. http://dx.doi.org/10.1016/s0969-806x(99)00523-x.

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12

Krishnan, Akhil R., H. Saleem, S. Subashchandrabose, N. Sundaraganesan, and S. Sebastain. "Molecular structure, vibrational spectroscopic (FT-IR, FT-Raman), UV and NBO analysis of 2-chlorobenzonitrile by density functional method." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 78, no. 2 (2011): 582–89. http://dx.doi.org/10.1016/j.saa.2010.11.027.

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13

Dwivedi, Ritambhara, Prabhakar Sharma, Akrati Sisodiya, Manohar Singh Batra, and Rajendra Prasad. "A DFT-assisted mechanism for evolution of the ammoxidation of 2-chlorotoluene (2-CLT) to 2-chlorobenzonitrile (2-CLBN) over alumina-supported V2O5 catalyst prepared by a solution combustion method." Journal of Catalysis 345 (January 2017): 245–57. http://dx.doi.org/10.1016/j.jcat.2016.10.033.

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14

Domingo, Luis R., та Nivedita Acharjee. "Unveiling the Chemo‐ and Regioselectivity of the [3+2] Cycloaddition Reaction between 4‐Chlorobenzonitrile Oxide and β‐Aminocinnamonitrile with a MEDT Perspective**". ChemistrySelect 6, № 18 (2021): 4521–32. http://dx.doi.org/10.1002/slct.202100978.

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15

Yang, Dong Sik, Ki-Cheol Son, and Stanley J. Kays. "Volatile Organic Compounds Emanating from Indoor Ornamental Plants." HortScience 44, no. 2 (2009): 396–400. http://dx.doi.org/10.21273/hortsci.44.2.396.

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A broad cross-section of volatiles emanating from four species of popular indoor ornamental plants (Spathiphyllum wallisii Regel, Sansevieria trifasciata Prain, Ficus benjamina L., and Chrysalidocarpus lutescens Wendl.) was identified and categorized based on source. Volatile organic compounds from individual plants were obtained using a dynamic headspace system and trapped on Tenax TA during the day and again at night. Using short-path thermal desorption and cryofocusing, the volatiles were transferred onto a capillary column and analyzed using gas chromatography–mass spectroscopy. The volati

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16

Sutherland, Ronald G., Chun-Hao Zhang, Adam Piórko, and Choi Chuck Lee. "Nucleophilic addition and substitution reactions between the cyanide ion and cyclopentadienyliron complexes of chlorobenzenes. Syntheses of benzonitriles and phthalonitriles." Canadian Journal of Chemistry 67, no. 1 (1989): 137–42. http://dx.doi.org/10.1139/v89-023.

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Reaction of cyclopentadienyliron (CpFe) complexes of chlorobenzenes with NaCN in DMF could give rise to products resulting from the addition of the cyanide ion or from substitution and addition reactions with the cyanide ion. Demetallation–oxidation of such products by treatment with DDQ would lead to the synthesis of benzonitriles and phthalonitriles. With the CpFe complex of chlorobenzene, reaction with NaCN in DMF for 3 min, 30 min, or 3 h gave rise to an approximately 90:10 mixture of (1–5-η5-1-chloro-exo-6-cyanocyclohexadienyl)(η5-cyclopentadienyl)iron (9) and (1–5-η5-1,exo-6-dicyanocyclo

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17

Tucker, Thomas J., John T. Sisko, Robert M. Tynebor, et al. "Discovery of 3-{5-[(6-Amino-1H-pyrazolo[3,4-b]pyridine-3-yl)methoxy]-2-chlorophenoxy}-5-chlorobenzonitrile (MK-4965): A Potent, Orally Bioavailable HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitor with Improved Potency against Key Mutant Viruses." Journal of Medicinal Chemistry 51, no. 20 (2008): 6503–11. http://dx.doi.org/10.1021/jm800856c.

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18

Gug, Fabienne, Stéphane Bach, Marc Blondel, Jean-Michel Vierfond, Anne-Sophie Martin, and Hervé Galons. "A single step synthesis of 6-aminophenanthridines from anilines and 2-chlorobenzonitriles." Tetrahedron 60, no. 21 (2004): 4705–8. http://dx.doi.org/10.1016/j.tet.2004.03.062.

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19

Mahajan, S. S., and A. Mahalakshmi. "Synthesis of 2-Amino-5-chlorobenzonitrile." ChemInform 37, no. 39 (2006). http://dx.doi.org/10.1002/chin.200639102.

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20

Ahmed, Riyadh M., Sarah S. Abdul Rahman, Dhefaf H. Badri, Khawla M. Sultan, Ismaeel Y. Majeed, and Ghada M. Kamil. "Synthesis, Characterisation and Biological Activity of New Co, Ni, Zn and Cd Polymeric Complexes Derived from Dithiocarbamate Ligand." Baghdad Science Journal, July 20, 2023. http://dx.doi.org/10.21123/bsj.2023.8038.

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Synthesis of a new class of Schiff-base ligand with a tetrazole moiety to form polymeric metal complexes with CoII, NiII, ZnII, and CdII ions has been demonstrated. The ligand was synthesised by a multi-steps by treating 5-amino-2-chlorobenzonitrile and cyclohexane -1,3-dione, the 5,5'-(((1E,3E)-cyclohexane-1,3-diylidene)bis(azanylylidene))bis(2-chlorobenzonitrile) was obtained. The precursor (M) was prepared from the reaction 5,5'-(((1E,3E)-cyclohexane-1,3-diylidene)bis(azanylylidene))bis(2-chlorobenzonitrile) with NaN3 to obtained (1E,3E)-N1,N3-bis(4-chloro-3-(1H-tetrazol-5-yl)phenyl)cyclohe

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21

Mahendra, Trivedi, Branton Alice, Trivedi Dahryn, and Nayak Gopal. "Experimental Investigation on Physical, Thermal and Spectroscopic Properties of 2-Chlorobenzonitrile: Impact of Biofield Treatment." Science Publishing Group, November 9, 2015. https://doi.org/10.5281/zenodo.813619.

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2-chlorobenzonitrile (2-ClBN) is widely used in the manufacturing of azo dyes, pharmaceuticals, and as intermediate in various chemical reactions. The aim of present study was to evaluate the impact of biofield treatment on physical, thermal and spectroscopic properties of 2-ClBN. 2-ClBN sample was divided into two groups that served as treated and control. The treated group received Mr. Trivedi's biofield treatment. Subsequently, the control and treated samples were evaluated using X-ray diffraction (XRD), surface area analyser, differential scanning calorimetry (DSC), thermogravimetric analy

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22

Gug, Fabienne, Stephane Bach, Marc Blondel, Jean-Michel Vierfond, Anne-Sophie Martin, and Herve Galons. "A Single Step Synthesis of 6-Aminophenanthridines from Anilines and 2-Chlorobenzonitriles." ChemInform 35, no. 37 (2004). http://dx.doi.org/10.1002/chin.200437141.

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23

Gadhave, Mahesh S., Soumen Barik, Felix Wessels, and Akkattu T. Biju. "Nucleophilic Acylation–Annulation Cascade of 2-Chlorobenzonitriles Using Aldehydes Triggered by N-Heterocyclic Carbenes." Organic Letters, November 14, 2023. http://dx.doi.org/10.1021/acs.orglett.3c03376.

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