4(S)-benzyl-3-<2(R)-<(tert-butoxycarbonyl)methyl>-4-phenylbutanoyl>-2-oxazolidinone

Base Information

Chemical Name:4(S)-benzyl-3-<2(R)-<(tert-butoxycarbonyl)methyl>-4-phenylbutanoyl>-2-oxazolidinone
CAS No.:188729-02-4
Molecular Formula:C₂₆H₃₁NO₅
Molecular Weight:437.536
Hs Code.:

Synonyms:4(S)-benzyl-3-<2(R)-<(tert-butoxycarbonyl)methyl>-4-phenylbutanoyl>-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 4(S)-benzyl-3-<2(R)-<(tert-butoxycarbonyl)methyl>-4-phenylbutanoyl>-2-oxazolidinone

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Technology Process of 4(S)-benzyl-3-<2(R)-<(tert-butoxycarbonyl)methyl>-4-phenylbutanoyl>-2-oxazolidinone

There total 4 articles about 4(S)-benzyl-3-<2(R)-<(tert-butoxycarbonyl)methyl>-4-phenylbutanoyl>-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: 59.0%

: 5292-43-3
bromoacetic acid tert-butyl ester

: 170450-77-8
(S)-4-benzyl-3-(3-phenylbutanoyl)oxazolidin-2-one

: 188729-02-4
4(S)-benzyl-3-<2(R)-<(tert-butoxycarbonyl)methyl>-4-phenylbutanoyl>-2-oxazolidinone

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; hexane; at -78 - 20 ℃;
DOI:10.1021/jm970404a

Reference yield:

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

: 188729-02-4
4(S)-benzyl-3-<2(R)-<(tert-butoxycarbonyl)methyl>-4-phenylbutanoyl>-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 25 min, 2.) THF, hexane, from -78 deg C to RT

2: 59 percent / LDA / tetrahydrofuran; hexane / -78 - 20 °C

With n-butyllithium; lithium diisopropyl amide; In tetrahydrofuran; hexane;
DOI:10.1021/jm970404a

Reference yield:

: 18496-54-3
phenylbutyric acid chloride

: 188729-02-4
4(S)-benzyl-3-<2(R)-<(tert-butoxycarbonyl)methyl>-4-phenylbutanoyl>-2-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-BuLi / 1.) THF, hexane, -78 deg C, 25 min, 2.) THF, hexane, from -78 deg C to RT

2: 59 percent / LDA / tetrahydrofuran; hexane / -78 - 20 °C

With n-butyllithium; lithium diisopropyl amide; In tetrahydrofuran; hexane;
DOI:10.1021/jm970404a