(R)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate

Base Information

Chemical Name:(R)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate
CAS No.:1316673-16-1
Molecular Formula:C₂₁H₁₇ClN₂O₄
Molecular Weight:396.83
Hs Code.:

Synonyms:(R)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate

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Chemical Property of (R)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate

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Technology Process of (R)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate

There total 2 articles about (R)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate 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:

: 941-69-5
N-phenyl-maleimide

: 147795-56-0,15032-43-6
ethyl 2-(4-chlorophenyl)-2-cyanoacetate

: 1316673-16-1
(R)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate

: (S)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((R)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate

Guidance literature:: With C₃₁H₅₃N₃O₂S; In toluene; at -30 ℃; for 2h; Overall yield = 96 %; enantioselective reaction;
DOI:10.1016/j.tetasy.2012.11.009

Reference yield:

: 941-69-5
N-phenyl-maleimide

: 147795-56-0,15032-43-6
ethyl 2-(4-chlorophenyl)-2-cyanoacetate

: 1316673-16-1
(R)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate

: (S)-ethyl 2-(4-chlorophenyl)-2-cyano-2-((R)-2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate

: ethyl 2-(4-chlorophenyl)-2-cyano-2-(2,5-dioxo-1-phenylpyrrolidin-3-yl)acetate

Guidance literature:: With C₃₇H₃₁F₆N₃S; In toluene; at 20 ℃; for 96h; Overall yield = 95 %; Optical yield = 84 %ee; stereoselective reaction;
DOI:10.1002/bkcs.10439