(2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol

Base Information

Chemical Name:(2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol
CAS No.:154799-20-9
Molecular Formula:C₁₉H₃₁NO₄
Molecular Weight:337.459
Hs Code.:

(2S,3R,4R)-2-<N-(tert-butoxycarbonyl)amino>-6-methyl-1-phenylheptane-3,4-diol

Synonyms:(2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol

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Chemical Property of (2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol

Chemical Property:

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Technology Process of (2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol

There total 3 articles about (2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol 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:

: 24424-99-5
di-tert-butyl dicarbonate

: 154799-20-9
(2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol

Guidance literature:: Multi-step reaction with 3 steps

1: CHCl₃ / 4 h

2: 1.) DMSO, COCl₂, 2.) Et₃N / 1.) CH₂Cl₂, -63 deg C, 20 min, 2.) CH₂Cl₂, -63 deg C, 20 min

With dimethyl sulfoxide; triethylamine; In chloroform;
DOI:10.1021/ja00083a017

Reference yield:

: 3182-95-4
L-Phenylalaninol

: 154799-20-9
(2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol

Guidance literature:: Multi-step reaction with 3 steps

1: CHCl₃ / 4 h

2: 1.) DMSO, COCl₂, 2.) Et₃N / 1.) CH₂Cl₂, -63 deg C, 20 min, 2.) CH₂Cl₂, -63 deg C, 20 min

With dimethyl sulfoxide; triethylamine; In chloroform;
DOI:10.1021/ja00083a017

Reference yield:

: 66605-57-0
(S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol

: 154799-20-9
(2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) DMSO, COCl₂, 2.) Et₃N / 1.) CH₂Cl₂, -63 deg C, 20 min, 2.) CH₂Cl₂, -63 deg C, 20 min

With dimethyl sulfoxide; triethylamine;
DOI:10.1021/ja00083a017