(1S,2R)-1-Benzoylamino-2-phenethyl-cyclopropanecarboxylic acid methyl ester

Base Information

Chemical Name:(1S,2R)-1-Benzoylamino-2-phenethyl-cyclopropanecarboxylic acid methyl ester
CAS No.:177540-25-9
Molecular Formula:C₂₀H₂₁NO₃
Molecular Weight:323.392
Hs Code.:

Synonyms:(1S,2R)-1-Benzoylamino-2-phenethyl-cyclopropanecarboxylic acid methyl ester

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Chemical Property of (1S,2R)-1-Benzoylamino-2-phenethyl-cyclopropanecarboxylic acid methyl ester

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Technology Process of (1S,2R)-1-Benzoylamino-2-phenethyl-cyclopropanecarboxylic acid methyl ester

There total 1 articles about (1S,2R)-1-Benzoylamino-2-phenethyl-cyclopropanecarboxylic 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: 100.0%

: (1S,2S)-1-Benzoylamino-2-((E)-styryl)-cyclopropanecarboxylic acid methyl ester

: 177540-25-9
(1S,2R)-1-Benzoylamino-2-phenethyl-cyclopropanecarboxylic acid methyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 8h; under 760 Torr;
DOI:10.1016/0040-4020(96)00218-9

Reference yield: 71.0%

: 177540-25-9
(1S,2R)-1-Benzoylamino-2-phenethyl-cyclopropanecarboxylic acid methyl ester

: (1S,2R)-1-Benzoylamino-2-(2-carboxy-ethyl)-cyclopropanecarboxylic acid methyl ester

Guidance literature:: With ruthenium trichloride; sodium periodate; In tetrachloromethane; water; acetonitrile; for 24h; Ambient temperature;
DOI:10.1016/0040-4020(96)00218-9

Reference yield:

: 177540-25-9
(1S,2R)-1-Benzoylamino-2-phenethyl-cyclopropanecarboxylic acid methyl ester

: 177540-27-1
(1S,2R)-1-amino-2-(2-α-phenethyl)cyclopropanecarboxylic acid

Guidance literature:: With hydrogenchloride; acetic acid; methyloxirane; Yield given. Multistep reaction; 1.) reflux, 40 h, 2.) ethanol, reflux, 30 min;
DOI:10.1016/0040-4020(96)00218-9