(2R,3S)-3-<(tert-butyloxycarbonyl)amino>-1-(phenylsulfinyl)-2-hydroxy-5-methylhexane

Base Information

Chemical Name:(2R,3S)-3-<(tert-butyloxycarbonyl)amino>-1-(phenylsulfinyl)-2-hydroxy-5-methylhexane
CAS No.:109996-67-0
Molecular Formula:C₁₈H₂₉NO₄S
Molecular Weight:355.499
Hs Code.:

Synonyms:(2R,3S)-3-<(tert-butyloxycarbonyl)amino>-1-(phenylsulfinyl)-2-hydroxy-5-methylhexane

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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,3S)-3-<(tert-butyloxycarbonyl)amino>-1-(phenylsulfinyl)-2-hydroxy-5-methylhexane

Chemical Property:

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Technology Process of (2R,3S)-3-<(tert-butyloxycarbonyl)amino>-1-(phenylsulfinyl)-2-hydroxy-5-methylhexane

There total 3 articles about (2R,3S)-3-<(tert-butyloxycarbonyl)amino>-1-(phenylsulfinyl)-2-hydroxy-5-methylhexane 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: 78.0%

: 109996-54-5
(2R,3S)-3-<(tert-butyloxycarbonyl)amino>-1-(phenylthio)-2-hydroxy-5-methylhexane

: 109996-67-0
(2R,3S)-3-<(tert-butyloxycarbonyl)amino>-1-(phenylsulfinyl)-2-hydroxy-5-methylhexane

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1021/jm00392a015

Reference yield:

: 108-98-5
thiophenol

: 109996-67-0
(2R,3S)-3-<(tert-butyloxycarbonyl)amino>-1-(phenylsulfinyl)-2-hydroxy-5-methylhexane

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / Et₃N / methanol / 2 h / Heating

2: 78 percent / 3-chloroperoxybenzoic acid (MCPBA) / CH₂Cl₂

With triethylamine; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane;
DOI:10.1021/jm00392a015

Reference yield:

: 107202-51-7
(2R)-2-[(1S)-1-[N-(tert-butyloxycarbonyl)amino]-3-methylbutyl]oxirane

: 109996-67-0
(2R,3S)-3-<(tert-butyloxycarbonyl)amino>-1-(phenylsulfinyl)-2-hydroxy-5-methylhexane

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / Et₃N / methanol / 2 h / Heating

2: 78 percent / 3-chloroperoxybenzoic acid (MCPBA) / CH₂Cl₂

With triethylamine; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane;
DOI:10.1021/jm00392a015