(4R)-(tert-butyldimethylsilanyloxy)-1-(2-cyanoethyl)pyrrolidin-(2S)-carboxylic acid allyl ester

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Chemical Name:(4R)-(tert-butyldimethylsilanyloxy)-1-(2-cyanoethyl)pyrrolidin-(2S)-carboxylic acid allyl ester
CAS No.:933469-70-6
Molecular Formula:C₁₇H₃₀N₂O₃Si
Molecular Weight:338.522
Hs Code.:

Synonyms:(4R)-(tert-butyldimethylsilanyloxy)-1-(2-cyanoethyl)pyrrolidin-(2S)-carboxylic acid allyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (4R)-(tert-butyldimethylsilanyloxy)-1-(2-cyanoethyl)pyrrolidin-(2S)-carboxylic acid allyl ester

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Technology Process of (4R)-(tert-butyldimethylsilanyloxy)-1-(2-cyanoethyl)pyrrolidin-(2S)-carboxylic acid allyl ester

There total 1 articles about (4R)-(tert-butyldimethylsilanyloxy)-1-(2-cyanoethyl)pyrrolidin-(2S)-carboxylic acid allyl 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:

: 40216-83-9
L-4-hydroxyproline methyl ester hydrochloride

: 933469-70-6
(4R)-(tert-butyldimethylsilanyloxy)-1-(2-cyanoethyl)pyrrolidin-(2S)-carboxylic acid allyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / triethylamine / CH₂Cl₂ / 12 h / Heating

2: 86 percent / 2,6-lutidine / 3 h / -20 °C

3: 58 percent / NaH / 48 h / Heating

With 2,6-dimethylpyridine; sodium hydride; triethylamine; In dichloromethane;
DOI:10.1016/j.tetlet.2007.01.046