(2S,3S,4S,5S)-methyl 5-(4-bromophenyl)-4 (2-methylpropanoyl)3-(phenylsulfonyl)pyrrolidine-2-carboxylate

Base Information

Chemical Name:(2S,3S,4S,5S)-methyl 5-(4-bromophenyl)-4 (2-methylpropanoyl)3-(phenylsulfonyl)pyrrolidine-2-carboxylate
CAS No.:1202390-05-3
Molecular Formula:C₂₂H₂₄BrNO₅S
Molecular Weight:494.406
Hs Code.:

Synonyms:(2S,3S,4S,5S)-methyl 5-(4-bromophenyl)-4 (2-methylpropanoyl)3-(phenylsulfonyl)pyrrolidine-2-carboxylate

Suppliers and Price of (2S,3S,4S,5S)-methyl 5-(4-bromophenyl)-4 (2-methylpropanoyl)3-(phenylsulfonyl)pyrrolidine-2-carboxylate

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

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Total 1 raw suppliers

Chemical Property of (2S,3S,4S,5S)-methyl 5-(4-bromophenyl)-4 (2-methylpropanoyl)3-(phenylsulfonyl)pyrrolidine-2-carboxylate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (2S,3S,4S,5S)-methyl 5-(4-bromophenyl)-4 (2-methylpropanoyl)3-(phenylsulfonyl)pyrrolidine-2-carboxylate

There total 1 articles about (2S,3S,4S,5S)-methyl 5-(4-bromophenyl)-4 (2-methylpropanoyl)3-(phenylsulfonyl)pyrrolidine-2-carboxylate 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: 59.0%

: 137958-30-6
(E)-4-methyl-1-(phenylsulfonyl)pent-1-en-3-one

: 139575-14-7
methyl 2-[(E)-[(4-bromophenyl)methylidene]amino]acetate

: C₂₂H₂₄BrNO₅S

: 1202390-05-3
(2S,3S,4S,5S)-methyl 5-(4-bromophenyl)-4 (2-methylpropanoyl)3-(phenylsulfonyl)pyrrolidine-2-carboxylate

Guidance literature:: With (R)-((4,4’-bi-1,3-benzodioxole)-5,5’-diyl)bis(bis(3,5-di-t-butyl-4-methoxyphenyl))phosphine; tetrakis(actonitrile)copper(I) hexafluorophosphate; triethylamine; In diethyl ether; at 20 ℃; for 21h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/jo902103z