(2S,3R)-2-<(tert-butyloxycarbonyl)amino>-1-cyclohexyl-3-hydroxy-6-methylheptan-4-one

Base Information

Chemical Name:(2S,3R)-2-<(tert-butyloxycarbonyl)amino>-1-cyclohexyl-3-hydroxy-6-methylheptan-4-one
CAS No.:114457-87-3
Molecular Formula:C₁₉H₃₅NO₄
Molecular Weight:341.491
Hs Code.:

Synonyms:(2S,3R)-2-<(tert-butyloxycarbonyl)amino>-1-cyclohexyl-3-hydroxy-6-methylheptan-4-one

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Chemical Property of (2S,3R)-2-<(tert-butyloxycarbonyl)amino>-1-cyclohexyl-3-hydroxy-6-methylheptan-4-one

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Technology Process of (2S,3R)-2-<(tert-butyloxycarbonyl)amino>-1-cyclohexyl-3-hydroxy-6-methylheptan-4-one

There total 5 articles about (2S,3R)-2-<(tert-butyloxycarbonyl)amino>-1-cyclohexyl-3-hydroxy-6-methylheptan-4-one 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: 96.0%

: ((1S,2R)-1-Cyclohexylmethyl-5-methyl-3-oxo-2-triethylsilanyloxy-hexyl)-carbamic acid tert-butyl ester

: 114457-87-3
(2S,3R)-2-<(tert-butyloxycarbonyl)amino>-1-cyclohexyl-3-hydroxy-6-methylheptan-4-one

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 0.25h;
DOI:10.1016/0040-4039(95)00824-V

Reference yield:

: 98105-42-1
(S)-2-(t-butoxycarbonylamino)-3-cyclohexyl-1-propanal

: 114457-87-3
(2S,3R)-2-<(tert-butyloxycarbonyl)amino>-1-cyclohexyl-3-hydroxy-6-methylheptan-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: ZnI₂ / CH₂Cl₂ / 1 h / Ambient temperature

2: CH₂Cl₂; diethyl ether / 4 h / Ambient temperature

With zinc(II) iodide; In diethyl ether; dichloromethane;
DOI:10.1021/jo00261a024

Reference yield:

: 103322-56-1
tert-butyl [(1S)-2-cyclohexyl-1-(hydroxymethyl)ethyl]carbamate

: 114457-87-3
(2S,3R)-2-<(tert-butyloxycarbonyl)amino>-1-cyclohexyl-3-hydroxy-6-methylheptan-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl chloride, DMSO, Et₃N / CH₂Cl₂ / 0.17 h

2: ZnI₂ / CH₂Cl₂ / 1 h / Ambient temperature

3: CH₂Cl₂; diethyl ether / 4 h / Ambient temperature

With oxalyl dichloride; dimethyl sulfoxide; triethylamine; zinc(II) iodide; In diethyl ether; dichloromethane;
DOI:10.1021/jo00261a024