(2R,3S)-3-Benzyloxycarbonylamino-2-methanesulfonyloxy-butyric acid tert-butyl ester

Base Information

Chemical Name:(2R,3S)-3-Benzyloxycarbonylamino-2-methanesulfonyloxy-butyric acid tert-butyl ester
CAS No.:203064-76-0
Molecular Formula:C₁₇H₂₅NO₇S
Molecular Weight:387.454
Hs Code.:

Synonyms:(2R,3S)-3-Benzyloxycarbonylamino-2-methanesulfonyloxy-butyric acid tert-butyl ester

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Chemical Property of (2R,3S)-3-Benzyloxycarbonylamino-2-methanesulfonyloxy-butyric acid tert-butyl ester

Chemical Property:

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Technology Process of (2R,3S)-3-Benzyloxycarbonylamino-2-methanesulfonyloxy-butyric acid tert-butyl ester

There total 3 articles about (2R,3S)-3-Benzyloxycarbonylamino-2-methanesulfonyloxy-butyric acid tert-butyl 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: 88.0%

: 124-63-0
methanesulfonyl chloride

: 203064-74-8
tert-butyl (2R,3S)-3-(((benzyloxy)carbonyl)amino)-2-hydroxybutanoate

: 203064-76-0
(2R,3S)-3-Benzyloxycarbonylamino-2-methanesulfonyloxy-butyric acid tert-butyl ester

Guidance literature:: With triethylamine; In dichloromethane;
DOI:10.1021/jo9720391

Reference yield:

: 621-84-1
O-benzyl carbamate

: 203064-76-0
(2R,3S)-3-Benzyloxycarbonylamino-2-methanesulfonyloxy-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

2: 88 percent / triethylamine / CH₂Cl₂

With triethylamine; In dichloromethane;
DOI:10.1021/jo9720391

Reference yield:

: 79218-15-8
tert-butyl (E)-crotonate

: 203064-76-0
(2R,3S)-3-Benzyloxycarbonylamino-2-methanesulfonyloxy-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

2: 88 percent / triethylamine / CH₂Cl₂

With triethylamine; In dichloromethane;
DOI:10.1021/jo9720391