(4S,2'S,3'R)-<1'-13C>-3-(2'-methyl-3'-hydroxypentanoyl)-4-benzyl-2-oxazolidinone

Base Information

Chemical Name:(4S,2'S,3'R)-<1'-13C>-3-(2'-methyl-3'-hydroxypentanoyl)-4-benzyl-2-oxazolidinone
CAS No.:145936-90-9
Molecular Formula:C₁₆H₂₁NO₄
Molecular Weight:292.336
Hs Code.:

Synonyms:(4S,2'S,3'R)-<1'-13C>-3-(2'-methyl-3'-hydroxypentanoyl)-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,2'S,3'R)-<1'-13C>-3-(2'-methyl-3'-hydroxypentanoyl)-4-benzyl-2-oxazolidinone

Chemical Property:

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Technology Process of (4S,2'S,3'R)-<1'-13C>-3-(2'-methyl-3'-hydroxypentanoyl)-4-benzyl-2-oxazolidinone

There total 2 articles about (4S,2'S,3'R)-<1'-13C>-3-(2'-methyl-3'-hydroxypentanoyl)-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:

: 90719-32-7
(S)-4-Benzyl-2-oxazolidinone

: 145936-90-9
(4S,2'S,3'R)-<1'-13C>-3-(2'-methyl-3'-hydroxypentanoyl)-4-benzyl-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: n-BuLi / tetrahydrofuran / -78 °C

2: 1.) i-Pr₂NEt, Bu₂BOTf, 3.) 30percent H₂O₂

With n-butyllithium; di-n-butylboryl trifluoromethanesulfonate; dihydrogen peroxide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran;
DOI:10.1021/ja00055a023

Reference yield:

: 123-38-6
propionaldehyde

: (4S)-3-<1'-13C>propionyl-4-benzyl-2-oxazolidinone

: 145936-90-9
(4S,2'S,3'R)-<1'-13C>-3-(2'-methyl-3'-hydroxypentanoyl)-4-benzyl-2-oxazolidinone

Guidance literature:: With di-n-butylboryl trifluoromethanesulfonate; dihydrogen peroxide; N-ethyl-N,N-diisopropylamine; Multistep reaction;
DOI:10.1021/ja00055a023