(2R)-1-(tert-butyloxycarbonyl)-2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(phenylsulfonyl)pyrrolidine

Base Information

Chemical Name:(2R)-1-(tert-butyloxycarbonyl)-2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(phenylsulfonyl)pyrrolidine
CAS No.:187409-52-5
Molecular Formula:C₂₂H₃₇NO₅SSi
Molecular Weight:455.691
Hs Code.:

Synonyms:(2R)-1-(tert-butyloxycarbonyl)-2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(phenylsulfonyl)pyrrolidine

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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 (2R)-1-(tert-butyloxycarbonyl)-2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(phenylsulfonyl)pyrrolidine

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Technology Process of (2R)-1-(tert-butyloxycarbonyl)-2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(phenylsulfonyl)pyrrolidine

There total 2 articles about (2R)-1-(tert-butyloxycarbonyl)-2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(phenylsulfonyl)pyrrolidine 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: 71.0%

: 103935-47-3
2-bromoethyl triflate

: 187409-49-0
(2R)-1-[(tert-butyldimethylsilyl)oxy]-2-[(tert-butyloxycarbonyl)amino]-3-(phenylsulfonyl)propane

: 187409-52-5
(2R)-1-(tert-butyloxycarbonyl)-2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(phenylsulfonyl)pyrrolidine

Guidance literature:: With n-butyllithium; In tetrahydrofuran; hexane; 1.) -78 deg C, 30 min, 2.) -78 deg C -> 0 deg C, 2 h;
DOI:10.1021/jo961790r

Reference yield:

: 116611-44-0
((R)-2-benzenesulfonyl-1-hydroxymethyl-ethyl)carbamic acid tert-butyl ester

: 187409-52-5
(2R)-1-(tert-butyloxycarbonyl)-2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(phenylsulfonyl)pyrrolidine

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent

2: 71 percent / n-BuLi / tetrahydrofuran; hexane / 1.) -78 deg C, 30 min, 2.) -78 deg C -> 0 deg C, 2 h

With n-butyllithium; In tetrahydrofuran; hexane;
DOI:10.1021/jo961790r

Reference yield:

: 106-95-6
allyl bromide

: 187409-52-5
(2R)-1-(tert-butyloxycarbonyl)-2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-(phenylsulfonyl)pyrrolidine

: (2R,3S)-1-(tert-butyloxycarbonyl)-2-{[(tert-butyldimethylsilyl)oxy]methyl}-3-allyl-3-(phenylsulfonyl)pyrrolidine

Guidance literature:: With n-butyllithium; Yield given. Multistep reaction; 1.) THF, hexane, -50 deg C, 30 min, 2.) THF, hexane, -78 deg C -> 0 deg C, 3 h;
DOI:10.1021/jo961790r