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Relevant bibliographies by topics / Ethyl Benzoates

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Dissertations / Theses
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Academic literature on the topic 'Ethyl Benzoates'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Ethyl Benzoates"

1

Gein, V. L., T. M. Zamaraeva, E. V. Gorgopina, and M. V. Dmitriev. "Biginelli reaction in the synthesis of ethyl 4-(6-aryl-5-benzoyl-4-hydroxy-2-thioxohexahydropyrimidine-4-carboxamido)benzoates." Журнал общей химии 93, no. 1 (2023): 43–49. http://dx.doi.org/10.31857/s0044460x23010055.

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Three-component Biginelli reaction of ethyl 4-(2,4-dioxo-4-phenylbutanamido)benzoate, aromatic aldehyde and thiourea in acetic acid in the presence of sodium acetate led to the formation of ethyl 4-(6-aryl-5-benzoyl4-hydroxy-2-thioxohexahydropyrimidine-4-carboxamido)benzoates. Structure of the obtained compounds was established by IR, 1H NMR, 13C spectroscopy methods.

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Sakai, Norio, Hiromu Maeda, and Yohei Ogiwara. "Copper-Catalyzed Three-Component Coupling Reaction of Aryl Iodides, a Disilathiane, and Alkyl Benzoates Leading to a One-Pot Synthesis of Alkyl Aryl Sulfides." Synthesis 51, no. 11 (2019): 2323–30. http://dx.doi.org/10.1055/s-0037-1610869.

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A copper-catalyzed three-component coupling reaction of aryl iodides, hexamethyldisilathiane and alkyl benzoates leading to alkyl aryl sulfides has been demonstrated. A disilathiane acted as both a sulfur source and a promoter of the sulfidation, and the alkyl moiety of the alkyl benzoate was effectively introduced on one side of the sulfide. Moreover, we found that the protocol can be expanded to the preparation of ethyl phenyl selenide with diphenyl diselenide.

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Dasmohapatra, Gourkrishna, Thomas Wolff, and Günther von Bünau. "Photochemistry in Porous Materials, II / Photolysis of Benzoin Ethers in Silicalite." Zeitschrift für Naturforschung B 47, no. 11 (1992): 1541–44. http://dx.doi.org/10.1515/znb-1992-1106.

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Four benzoin ethers 1 (a: methyl-, b: ethyl-, c: isopropyl-, d: phenylether) were photolyzed inside the channel system of silicalite S- 115, a novel type of zeolite. Products which could be separated from the zeolite framework in various relative yields were pinacol ethers (from a, b, c), benzil (a–d), benzaldehyde (a–d), benzoates (a–d), and phenol (d). While the former three types of products clearly arise from Norrish type I cleavage of the parent molecules, a mechanism involving the enolic form of the benzoin ethers is proposed in order to explain the formation of benzoates and phenol.

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Nummert, Vilve, Mare Piirsalu, Vahur Mäemets, and Ilmar Koppel. "Kinetic Study of Hydrolysis of Benzoates. Part XXV. Ortho Substituent Effect in Alkaline Hydrolysis of Phenyl Esters of Substituted Benzoic Acids in Water." Collection of Czechoslovak Chemical Communications 71, no. 1 (2006): 107–28. http://dx.doi.org/10.1135/cccc20060107.

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The second-order rate constants k2 for alkaline hydrolysis of phenyl esters of meta-, para- and ortho-substituted benzoic acids, X-C6H4CO2C6H5 (X = H, 3-Cl, 3-NO2, 3-CH3, 4-NO2, 4-Cl, 4-F, 4-CH3, 4-OCH3, 4-NH2, 2-NO2, 2-CN, 2-F, 2-Cl, 2-Br, 2-I, 2-CH3, 2-OCH3, 2-CF3, 2-NH2), and of substituted phenyl esters of benzoic acid, C6H5CO2C6H4-X (X = 2-I, 2-CF3, 2-C(CH3)3, 4-Cl, 4-CH3, 4-OCH3, 4-NH2), have been measured spectrophotometrically in water at 25 °C. The substituent effect in alkaline hydrolysis of phenyl esters of para-substituted benzoic acids, similar to that for ethyl esters of para-sub

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Kim, In-Hae, and Eiichi Kuwano. "Synthesis and Insect Growth Regulating Activity of Ethyl Meta-Substituted Benzoates." Journal of the Faculty of Agriculture, Kyushu University 45, no. 2 (2001): 509–18. http://dx.doi.org/10.5109/24401.

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6

Campbell, M., DJ Collins, and AM James. "Synthesis of 2-(5',5'-Ethylenedioxy-1'-methylcyclopent-2'-en-1'-yl)ethanol, and Some 2H-Cyclopenta[b]furan Derivatives Formed by Intramolecular Displacement Reactions." Australian Journal of Chemistry 42, no. 1 (1989): 17. http://dx.doi.org/10.1071/ch9890017.

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Exchange dioxolanation of 2-methyl-2-(prop-2′-enyl)cyclopentane-1,3-done (1b) gave 3,3- ethylenedioxy-2-methyl-2-(prop-2′-enyl) cyclopentan-1-one (2) which, upon reduction and esterification , afforded the epimeric 3,3-ethylenedioxy-2-methyl-2-(prop-2′-enyl) cyclopent-1-yl benzoates (6d). Oxidative cleavage of the terminal double bond in (6d),followed by sodium borohydride reduction yielded 3,3-ethylenedioxy-2-(2'-hydroxyethyl)-2-methylcyclopent-1-yl benzoate (4b) which underwent acid- catalysed rearrangement to 6a-(2′-hydroxyethoxy)-3a- methylhexahydrocyclopenta [b]furan-4-yl benzoate (8b). F

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Vasu, A. Edwin, K. Joseph Santhanaraj, and S. Raja. "Reactions of Chlorine Gas on Benzaldehyde-di-n-alkyl Acetals." E-Journal of Chemistry 5, no. 2 (2008): 251–56. http://dx.doi.org/10.1155/2008/178560.

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Reactions of chlorine gas on six aromatic acetals, the benzaldehyde di-n-alkyl acetals, C6H4-CH(OR)2where R=ethyl (1a),n-propyl (2a),n-butyl (3a), isobutyl (4a),n-amyl (5a) and isoamyl (6a) were studied. The products were analyzed by IR and 1H NMR spectroscopic techniques and were found to be ring chlorinated alkyl benzoates. A plausible mechanism has been proposed based on the experimental observations and the effect of the alkyl groups on the product yield.

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FURUTA, Kenjiro, Hiromitsu SHIRAHASHI, Haruna YAMASHITA, Kiyo ASHIBE, and Eiichi KUWANO. "Synthesis and Anti-Juvenile Hormone Activity of Ethyl 4-(2-Aryloxyhexyloxy)benzoates." Bioscience, Biotechnology, and Biochemistry 70, no. 3 (2006): 746–48. http://dx.doi.org/10.1271/bbb.70.746.

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Mehmood, Hasnain, Zahoor Ahmad, Tashfeen Akhtar, et al. "Design, synthesis and liquid crystalline behavior of ethyl 4-((4-alkoxyphenyl)diazenyl)benzoates." Molecular Crystals and Liquid Crystals 664, no. 1 (2018): 14–23. http://dx.doi.org/10.1080/15421406.2018.1442779.

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Morley, Krista, and James A. Pincock. "The Photochemistry of 2-(1-Naphthyl)ethyl Benzoates: Cycloaddition and Intramolecular Exciplex Formation." Journal of Organic Chemistry 66, no. 9 (2001): 2995–3003. http://dx.doi.org/10.1021/jo001633z.

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Dissertations / Theses on the topic "Ethyl Benzoates"

1

Mitambo, Munyao Musilli. "Probing solute-solvent interactions in ethyl 4-(dimethylamino)benzoate with Raman spectroscopy." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0007/MQ59851.pdf.

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Rameesdeen, Sabra Banu. "Investigation of the ketonization reaction of renewable acids and esters." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2022. http://amslaurea.unibo.it/25424/.

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Ketonization is a promising reaction for the upgrading of bio oils produced from biomass and it is used for the preparation of highly valuable asymmetrical ketones such as di-hydrocalchone (HC) and acetyl furan (Ac-Fur). But, they are produced in the liquid-phase with poorly sustainable processes, e.g. Friedel-Crafts acylations (Ac-Fur) and tandem acylation/alkylation (HC) with homogeneous Lewis acid catalysts or oxidations with organic peroxides and excess MnO2 (HC) or H2O2 and inorganic homogeneous catalysts. The development of an alternative gas-phase process to produce HC and Et-Fur by mea

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Aqar, Dhia Y. "Modelling and Optimization of Conventional and Unconventional Batch Reactive Distillation Processes. Investigation of Different Types Batch Reactive Distillation Columns for the Production of a Number of Esters such as Methyl Lactate, Methyl Decanoate, Ethyl Benzoate, and Benzyl Acetate using gPROMS." Thesis, University of Bradford, 2018. http://hdl.handle.net/10454/17139.

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The synthesis of a number of alkyl esters such as methyl lactate, methyl decanoate, and ethyl benzoate via esterification in a reactive distillation is quite challenging. It is due to the complexity in the thermodynamic behaviour of the chemical species in the reaction mixture in addition to the difficulty of keeping the reactants together in the reaction section. One of the reactants (in these esterification reactions) having the lowest boiling point can separate from the other reactant as the distillation continues. This can result in a significant drop in the reaction conversion in a conven

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4

chou, Pei Lin, and 周珮琳. "Kinetics for Synthesis and Hydrolysis of Ethyl Benzoate." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/34503079619041470427.

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碩士<br>國立臺灣科技大學<br>化學工程系<br>91<br>The kinetic behavior of synthesis and hydrolysis of ethyl benzoate over an acidic cation-exchange resin, Amberlyst 39, was investigated with a fixed-bed reactor. The esterification was peformed at temperatures between 323.15 K and 353.15 K and molar ratios of feed ΘB0 (ethanol to benzoic acid) from 5 to 9. The hydrolysis was conducted also at temperatures between 323.15 K and 353.15 K, and the molar ratios of feed ΘC0´ (ethyl benzoate to water) from 0.5 to 8 and ΘB0 ´ (ethanol to water) from 1 to 7.42. The equilibrium conversion of benzoic acid was

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Aqar, D. Y., Nejat Rahmanian, and Iqbal M. Mujtaba. "Feasibility of Integrated Batch Reactive Distillation Columns for the Optimal Synthesis of Ethyl Benzoate." 2017. http://hdl.handle.net/10454/13170.

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Yes<br>The synthesis of ethyl benzoate (EtBZ) via esterification of benzoic acid (BeZ) with ethanol in a reactive distillation is challenging due to complex thermodynamic behaviour of the chemical reaction and the difficulty of keeping the reactants together in the reaction zone (ethanol having the lowest boiling point can separate from the BeZ as the distillation proceeds) causing a significant decrease in the conversion of BeZ in a conventional reactive distillation column (batch or continuous). This might be the reason of not reporting the use of reactive distillation for EtBZ synthesis alt

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6

李宇鈞. "Synthesis and Antiplatelet Activity of Ethyl 4-(1-phenyl-1H-indazol-3-yl)benzoate Analogues." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/17336074864915650784.

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碩士<br>中國醫藥學院<br>藥物化學研究所<br>90<br>Recently, ethyl 4-(1-benzyl-1H-indazol-3-yl)benzoate (YD-3) has been recognized as a representative of a new class of thrombin receptor antagonist, with unique mechanism of action. Encouraged by the initial result, a series of 1-phenyl analogs (6, 9, 10) was synthesized. The starting material ethyl 4-benzoylbenzoate (3) was treated with phenylhydrazine to yield the ethyl 4-[(phenylhydrazono)(phenyl)methyl] benzoate (4) as a mixture of E- and Z- form isomers. Then compound 4 was then treated with lead tetraacetate in dichloromethane at low

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7

Chen, Hua-Sin, and 陳華鑫. "Synthesis and biological activities of ethyl 4-(1-benzyl-1H-indazol-3-yl)benzoate (YD-3) derivative." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/47453222969722384672.

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博士<br>中國醫藥大學<br>藥物化學研究所<br>96<br>In the previous study, ethyl 4-(1-benzyl-1H-indazol-3-yl)benzoate (YD-3) was identified as the first selective non-peptide protease-activated receptor 4 (PAR4) antagonist. In order to develop noel PAR4 antagonist, YD-3 was selected as lead compound. Two series of N1-substituted arylmethyl-3-(4-ethoxycarbonylphenyl)indazole derivatives (I) and N2-substituted arylmethyl-3-(4-ethoxycarbonylphenyl)indazole derivatives (II) were synthesized. The key intermediate, ethyl 4-(1H-indazol-3-yl)- benzoate (8) was prepared according to the know method. Then, compound 8

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8

Chen, Hua-Sin, and 陳華鑫. "Synthesis and Antiplatelet Activity of Ethyl 4-(1-benzyl-1H-indazol-3-yl)benzoate (YD-3) Analogues." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/14381104464913170994.

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碩士<br>中國醫藥學院<br>藥物化學研究所<br>90<br>Ethyl 4-(1-benzyl-1H-indazol-3-yl)benzoate (YD-3) was first synthesized in our laboratory as a novel thrombin-receptor antagonist. In this study, YD-3 was used as a lead compound and a series of its derivatives (9a—9d, 10a—10n) were prepared. The key intermediate YD-3, was synthesized according to Scheme 6. The starting material ethyl 4-benzoylbenzoate (3) was treated with benzylhydrazine to yield ethyl 4-[(benzylhydrazono)(phenyl)methyl] benzoate (4) as a mixture of E- and Z-form isomers. The hydrazone was then treated with lead tetraacet

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Book chapters on the topic "Ethyl Benzoates"

1

Lide, David R. "Ethyl benzoate." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-212.

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2

Gooch, Jan W. "Ethyl Benzoate." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_4548.

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3

Bährle-Rapp, Marina. "Ethyl Benzoate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3706.

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4

Wohlfarth, Ch. "Viscosity of ethyl benzoate." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_318.

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Wohlfarth, Christian. "Viscosity of ethyl benzoate." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_318.

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Wohlfarth, Ch. "Dielectric constant of ethyl benzoate." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_280.

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7

Wohlfarth, Ch. "Surface tension of ethyl benzoate." In Supplement to IV/16. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75508-1_166.

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8

Wohlfarth, Christian. "Refractive index of ethyl benzoate." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_335.

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9

Wohlfarth, Ch. "Refractive index of ethyl benzoate." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38). Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_285.

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10

Wohlfarth, Christian. "Static dielectric constant of ethyl benzoate." In Static Dielectric Constants of Pure Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-48168-4_186.

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Conference papers on the topic "Ethyl Benzoates"

1

Guan, Chang, Yu-Ying Zhou, and Qun Liu. "APPLICATION PROPERTIES OF ETHYL BENZOATE: ENVIRONMENTAL-FRIENDLY DYEING CARRIER FOR POLYESTER FIBER." In International Conference on New Materials and Intelligent Manufacturing (ICNMIM). Volkson Press, 2018. http://dx.doi.org/10.26480/icnmim.01.2018.161.163.

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2

Johnson, Folayan Adewale, Adewale Dosunmu, and Oriji Boniface Aleruchi. "Environmental Impact Assessment of Current Synthetic Drilling Fluids in Offshore Oil Fields Using Modified CO2 Evolution Respirometry Technique." In SPE Nigeria Annual International Conference and Exhibition. SPE, 2023. http://dx.doi.org/10.2118/217180-ms.

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Abstract Synthetic fluid biodegradation test is one of the essential requirements by environmental regulatory agencies before an approval for offshore cuttings disposal can be granted. In this study, the aerobic biodegradation tendencies of two industry grade, deep-water synthetic hydrocarbon-based fluids (SHBF and SEBF) were investigated using modified carbon-IV-oxide (CO2) evolution respirometry technique. The results were compared with an ester synthetic fluid that was code-named as ternary mixture of synthetic ethyl esters of plants oil (SEEP-Mixture). A known concentration of the test dri

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