(R)-2-Benzyloxycarbonylamino-4-methanesulfonyloxy-butyric acid methyl ester

Base Information

Chemical Name:(R)-2-Benzyloxycarbonylamino-4-methanesulfonyloxy-butyric acid methyl ester
CAS No.:637008-56-1
Molecular Formula:C₁₄H₁₉NO₇S
Molecular Weight:345.373
Hs Code.:

Synonyms:(R)-2-Benzyloxycarbonylamino-4-methanesulfonyloxy-butyric acid methyl ester

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Chemical Property of (R)-2-Benzyloxycarbonylamino-4-methanesulfonyloxy-butyric acid methyl ester

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Technology Process of (R)-2-Benzyloxycarbonylamino-4-methanesulfonyloxy-butyric acid methyl ester

There total 3 articles about (R)-2-Benzyloxycarbonylamino-4-methanesulfonyloxy-butyric 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:

: 1152-62-1,4434-61-1,28862-80-8
(2R)-2-[[(benzyloxy)carbonyl]amino]-4-(methylsulfanyl)butanoic acid

: 637008-56-1
(R)-2-Benzyloxycarbonylamino-4-methanesulfonyloxy-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen fluoride; methyl iodide / acetic acid / 15 h

2.1: potassium hydroxide / methanol / 18 h / 20 °C

2.2: 27 / 66 h / 20 °C

3.1: triethylamine / dichloromethane / 2 h / 0 °C

With potassium hydroxide; hydrogen fluoride; triethylamine; methyl iodide; In methanol; dichloromethane; acetic acid;
DOI:10.1139/v03-122

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 637008-56-1
(R)-2-Benzyloxycarbonylamino-4-methanesulfonyloxy-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydrogencarbonate / 22 h / 20 °C

2.1: hydrogen fluoride; methyl iodide / acetic acid / 15 h

3.1: potassium hydroxide / methanol / 18 h / 20 °C

3.2: 27 / 66 h / 20 °C

4.1: triethylamine / dichloromethane / 2 h / 0 °C

With potassium hydroxide; hydrogen fluoride; sodium hydrogencarbonate; triethylamine; methyl iodide; In methanol; dichloromethane; acetic acid;
DOI:10.1139/v03-122

Reference yield:

: 41088-89-5
D-2-<(benzyloxycarbonyl)amino>-4-butyrolactone

: 637008-56-1
(R)-2-Benzyloxycarbonylamino-4-methanesulfonyloxy-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium hydroxide / methanol / 18 h / 20 °C

1.2: 27 / 66 h / 20 °C

2.1: triethylamine / dichloromethane / 2 h / 0 °C

With potassium hydroxide; triethylamine; In methanol; dichloromethane;
DOI:10.1139/v03-122