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Ethyl 2-(4-chlorophenyl)-2-phenylacetate is an organic compound with the chemical formula C17H15ClO2. It is a colorless to pale yellow liquid with a molecular weight of 286.74 g/mol. ethyl 2-(4-chlorophenyl)-2-phenylacetate is characterized by the presence of a 4-chlorophenyl group and a phenyl group attached to a central acetate moiety, which is esterified with an ethyl group. It is synthesized through the esterification of 2-(4-chlorophenyl)-2-phenylacetic acid with ethanol. Ethyl 2-(4-chlorophenyl)-2-phenylacetate is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. Its chemical structure and properties make it a versatile building block in organic synthesis, allowing for further functionalization and the creation of a range of derivatives with diverse applications.

5359-54-6

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5359-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5359-54-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5359-54:
(6*5)+(5*3)+(4*5)+(3*9)+(2*5)+(1*4)=106
106 % 10 = 6
So 5359-54-6 is a valid CAS Registry Number.

5359-54-6Downstream Products

5359-54-6Relevant academic research and scientific papers

Photoredox Catalytic Phosphite-Mediated Deoxygenation of α-Diketones Enables Wolff Rearrangement and Staudinger Synthesis of β-Lactams

Jiang, Zhiyong,Li, Haijun,Wei, Guo,Yang, Hui

supporting information, p. 19696 - 19700 (2021/08/03)

A novel visible-light-driven catalytic activation of C=O bonds by exploiting the photoredox chemistry of 1,3,2-dioxaphospholes, readily accessible from α-diketones and trialkyl phosphites, is reported. This mild and environmentally friendly strategy provides an unprecedented and efficient access to the Wolff rearrangement reaction which traditionally entails α-diazoketones as precursors. The resulting ketenes could be precisely trapped by alcohols/thiols to give α-aryl (thio)acetates and by imines to afford the valuable β-lactams in up to 99 % yields.

Catalytic C-C coupling of diazo compounds with arylboronic acids: Using surface modified sewage sludge as catalyst

Huang, Fei,Huang, He,Hughes, Timothy,Xie, Yuxing,Xu, Jun,Yu, Yang,Zhang, Zhipeng

, p. 4165 - 4173 (2020/07/14)

A green, mild and efficient synthesis of diarylmethines using sewage sludge-derived carbonaceous materials (SW) by perchloric acid catalyzed coupling reactions between diazo compounds and arylboronic acids was developed. The reaction shows a high level of functional tolerance and a broad substrate scope. Furthermore, the highly selective 1,2-alkyl shift products were furnished through the sterically demanding R4, R5 migration of diazo compounds (3-diazochromanone). The structures of 1,2-shift products have been further confirmed by single-crystal X-ray analysis. Significantly, the synthesis of the core structures of darifenacin (a clinical drug for overactive bladder syndrome, OAB) and diclofensine (a stimulant drug showing antidepressant and monoamine reuptake inhibitor activity) further demonstrated the efficacy and synthetic potential of this method. This journal is

Method for synthesizing aryl acetate derivative under catalysis of surface modified sludge charcoal

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Paragraph 0066-0068, (2019/11/12)

The invention discloses a method for synthesizing an aryl acetate derivative under the catalysis of surface modified sludge charcoal. According to the method, the construction of a C-C bond is realized by an arylation reaction realized by taking the surfa

Rh(I)-catalyzed cross-coupling of α-diazoesters with arylsiloxanes

Xia, Ying,Liu, Zhen,Feng, Sheng,Ye, Fei,Zhang, Yan,Wang, Jianbo

supporting information, p. 956 - 959 (2015/03/30)

An Rh(I)-catalyzed cross-coupling of diazoesters with arylsiloxanes has been successfully achieved. This transformation is a new method for the construction of the C(sp3)-C(sp2) bond, thus providing an alternative synthesis of α-aryl esters. Rh(I)-carbene migratory insertion has been proposed to be involved in this coupling reaction. The reaction represents the first example of utilizing arylsiloxane as the coupling partner in the carbene-involved cross-coupling reactions.

Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins

Kothapalli, Raveendra Babu,Niddana, Ramana,Balamurugan, Rengarajan

supporting information, p. 1278 - 1281 (2014/04/03)

A simple protocol for the synthesis of α-diarylacetic esters from benzoins is described. In situ generated acetal assists rapid 1,2-aryl migration in a stereospecific manner, paving the way to make enantioenriched α-diarylacetic esters from easily accessi

PHOTOOXYDATION AND PHOTOOXYGENATION OF α-DIAZOKETONE IN ALCOHOL

Tomioka, Hideo,Kondo, Shingo,Misaki, Kiyotsugu,Izawa, Yasuji

, p. 2191 - 2194 (2007/10/02)

The investigation of the mechanism of oxydative-cleavage reaction of azibenzil in alcohol to give benzoates revealed the role of oxygen (either 1O2 or 3O2) in the photolysis of α-diazoketone-

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