(+)-(4S)-3-<(2'R)-2'-((tert-Butyldimethylsiloxy)methyl)butanoyl>-4-benzyl-2-oxazolidinone

Base Information

Chemical Name:(+)-(4S)-3-<(2'R)-2'-((tert-Butyldimethylsiloxy)methyl)butanoyl>-4-benzyl-2-oxazolidinone
CAS No.:157405-12-4
Molecular Formula:C₂₁H₃₃NO₄Si
Molecular Weight:391.583
Hs Code.:

Synonyms:(+)-(4S)-3-<(2'R)-2'-((tert-Butyldimethylsiloxy)methyl)butanoyl>-4-benzyl-2-oxazolidinone

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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 (+)-(4S)-3-<(2'R)-2'-((tert-Butyldimethylsiloxy)methyl)butanoyl>-4-benzyl-2-oxazolidinone

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Technology Process of (+)-(4S)-3-<(2'R)-2'-((tert-Butyldimethylsiloxy)methyl)butanoyl>-4-benzyl-2-oxazolidinone

There total 3 articles about (+)-(4S)-3-<(2'R)-2'-((tert-Butyldimethylsiloxy)methyl)butanoyl>-4-benzyl-2-oxazolidinone 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: 100.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 150615-45-5
(+)-(4S)-3-<(2'R)-2'-(hydroxymethyl)butanoyl>-4-benzyl-2-oxazolidinone

: 157405-12-4
(+)-(4S)-3-<(2'R)-2'-((tert-Butyldimethylsiloxy)methyl)butanoyl>-4-benzyl-2-oxazolidinone

Guidance literature:: With dmap; triethylamine; In dichloromethane; for 5h; Ambient temperature;
DOI:10.1021/jo951653e

Reference yield:

: 111292-87-6,143097-11-4,112459-79-7
(S)-4-benzyl-3-butyryloxazolidin-2-one

: 157405-12-4
(+)-(4S)-3-<(2'R)-2'-((tert-Butyldimethylsiloxy)methyl)butanoyl>-4-benzyl-2-oxazolidinone

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) TiCl₄, Et₃N / 1) CH₂Cl₂, 40 min, 0 deg C; 2) CH₂Cl₂, 0 deg C, 2 h

2: 100 percent / H₂ / Pd on carbon / ethanol / 72 h / Ambient temperature

3: 100 percent / 4-(N,N-dimethylamino)pyridine, Et₃N / CH₂Cl₂ / 5 h / Ambient temperature

With dmap; hydrogen; titanium tetrachloride; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1021/jo951653e

Reference yield:

: 163457-34-9
(+)-(4S)-3-<(2'R)-2'-((benzyloxy)methyl)butanoyl>-4-benzyl-2-oxazolidinone

: 157405-12-4
(+)-(4S)-3-<(2'R)-2'-((tert-Butyldimethylsiloxy)methyl)butanoyl>-4-benzyl-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / H₂ / Pd on carbon / ethanol / 72 h / Ambient temperature

2: 100 percent / 4-(N,N-dimethylamino)pyridine, Et₃N / CH₂Cl₂ / 5 h / Ambient temperature

With dmap; hydrogen; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1021/jo951653e