(1S,2S)-(E)-4-[N-(tert-butyloxycarbonyl)amino]-1,5-diphenylpent-1-en-3-ol

Base Information

Chemical Name:(1S,2S)-(E)-4-[N-(tert-butyloxycarbonyl)amino]-1,5-diphenylpent-1-en-3-ol
CAS No.:213603-02-2
Molecular Formula:C₂₂H₂₇NO₃
Molecular Weight:353.461
Hs Code.:

Synonyms:(1S,2S)-(E)-4-[N-(tert-butyloxycarbonyl)amino]-1,5-diphenylpent-1-en-3-ol

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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 (1S,2S)-(E)-4-[N-(tert-butyloxycarbonyl)amino]-1,5-diphenylpent-1-en-3-ol

Chemical Property:

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Technology Process of (1S,2S)-(E)-4-[N-(tert-butyloxycarbonyl)amino]-1,5-diphenylpent-1-en-3-ol

There total 2 articles about (1S,2S)-(E)-4-[N-(tert-butyloxycarbonyl)amino]-1,5-diphenylpent-1-en-3-ol 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:

: 213603-00-0
(4S,5S)-4-Benzyl-5-((E)-styryl)-oxazolidin-2-one

: 213603-02-2
(1S,2S)-(E)-4-[N-(tert-butyloxycarbonyl)amino]-1,5-diphenylpent-1-en-3-ol

Guidance literature:: Multi-step reaction with 2 steps

1: KOH / ethanol; H₂O / 19 h / Heating

2: CH₂Cl₂ / 3.5 h / 23 °C

With potassium hydroxide; In ethanol; dichloromethane; water;
DOI:10.1021/jo980159i

Reference yield:

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

: (E)-(3S,4S)-4-Amino-1,5-diphenyl-pent-1-en-3-ol

: 213603-02-2
(1S,2S)-(E)-4-[N-(tert-butyloxycarbonyl)amino]-1,5-diphenylpent-1-en-3-ol

Guidance literature:: In dichloromethane; at 23 ℃; for 3.5h; Yield given;
DOI:10.1021/jo980159i

Reference yield:

: 213603-02-2
(1S,2S)-(E)-4-[N-(tert-butyloxycarbonyl)amino]-1,5-diphenylpent-1-en-3-ol

: 98760-08-8
(2R,3S)-3-[N-(tert-butyloxycarbonyl)amino]-1,2-epoxy-4-phenylbutane

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) O₃, 2.) NaBH₄ / 1.) EtOH, -78 deg C, 45 min, 2.) EtOH, 23 deg C, 1 h

2: 88 percent / PPh₃, DEAD / CHCl₃ / 50 h / Heating

With sodium tetrahydroborate; ozone; triphenylphosphine; diethylazodicarboxylate; In chloroform;
DOI:10.1021/jo980159i