(1R,2S)-2-(4-Chloro-phenyl)-cyclopropane-1,1-dicarboxylic acid methyl ester

Base Information

Chemical Name:(1R,2S)-2-(4-Chloro-phenyl)-cyclopropane-1,1-dicarboxylic acid methyl ester
CAS No.:97364-80-2
Molecular Formula:C₁₂H₁₁ClO₄
Molecular Weight:254.67
Hs Code.:

Synonyms:(1R,2S)-2-(4-Chloro-phenyl)-cyclopropane-1,1-dicarboxylic acid methyl ester

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Chemical Property of (1R,2S)-2-(4-Chloro-phenyl)-cyclopropane-1,1-dicarboxylic acid methyl ester

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Technology Process of (1R,2S)-2-(4-Chloro-phenyl)-cyclopropane-1,1-dicarboxylic acid methyl ester

There total 1 articles about (1R,2S)-2-(4-Chloro-phenyl)-cyclopropane-1,1-dicarboxylic acid methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 75.0%

: 97381-36-7
1-(4-Chloro-phenyl)-6,6-dimethyl-5,7-dioxa-spiro[2.5]octane-4,8-dione

: 97364-80-2
(1R,2S)-2-(4-Chloro-phenyl)-cyclopropane-1,1-dicarboxylic acid methyl ester

Guidance literature:: With sodium methylate; In methanol; for 3h;
DOI:10.1016/S0040-4020(01)83489-X

Reference yield:

: 97364-80-2
(1R,2S)-2-(4-Chloro-phenyl)-cyclopropane-1,1-dicarboxylic acid methyl ester

: 97364-31-3
(1S,2S)-2-(4-Chloro-phenyl)-1-isocyanato-cyclopropanecarboxylic acid methyl ester

Guidance literature:: With sodium azide; chloroformic acid ethyl ester; ethyl azide; Yield given. Multistep reaction; 1.) acetone, H₂O, 30 min; 2.) acetone, H₂O, 1 h; 3.) toluene, reflux, 3 h;
DOI:10.1016/S0040-4020(01)83489-X

Reference yield:

: 97364-80-2
(1R,2S)-2-(4-Chloro-phenyl)-cyclopropane-1,1-dicarboxylic acid methyl ester

: 63141-02-6,97364-39-1,97364-40-4
acide amino-1 parachlorophenyl-2 cyclopropanecarboxylique trans chlorhydrate

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) EtN₃, ethylchloroformate; 2.) NaN₃ / 1.) acetone, H₂O, 30 min; 2.) acetone, H₂O, 1 h; 3.) toluene, reflux, 3 h

2: 54 percent / 6M HCl / 8 h / Heating

With hydrogenchloride; sodium azide; chloroformic acid ethyl ester; ethyl azide;
DOI:10.1016/S0040-4020(01)83489-X