(1Z,3S,4S,5S)-5-Benzyloxy-4-hydroxy-3-methyl-1-hexenyl N,N-diisopropylcarbamate

Base Information

Chemical Name:(1Z,3S,4S,5S)-5-Benzyloxy-4-hydroxy-3-methyl-1-hexenyl N,N-diisopropylcarbamate
CAS No.:110455-86-2
Molecular Formula:C₂₁H₃₃NO₄
Molecular Weight:363.497
Hs Code.:

Synonyms:(1Z,3S,4S,5S)-5-Benzyloxy-4-hydroxy-3-methyl-1-hexenyl N,N-diisopropylcarbamate

Suppliers and Price of (1Z,3S,4S,5S)-5-Benzyloxy-4-hydroxy-3-methyl-1-hexenyl N,N-diisopropylcarbamate

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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 (1Z,3S,4S,5S)-5-Benzyloxy-4-hydroxy-3-methyl-1-hexenyl N,N-diisopropylcarbamate

Chemical Property:

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Technology Process of (1Z,3S,4S,5S)-5-Benzyloxy-4-hydroxy-3-methyl-1-hexenyl N,N-diisopropylcarbamate

There total 3 articles about (1Z,3S,4S,5S)-5-Benzyloxy-4-hydroxy-3-methyl-1-hexenyl N,N-diisopropylcarbamate 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:

: 54783-72-1
ethyl (S)-2-(benzyloxy)propionate

: 110455-86-2
(1Z,3S,4S,5S)-5-Benzyloxy-4-hydroxy-3-methyl-1-hexenyl N,N-diisopropylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: DIBAH / diethyl ether

With diisobutylaluminium hydride; In diethyl ether;
DOI:10.1055/s-1989-27159

Reference yield:

: 81445-44-5
(S)-2-(benzyloxy)propanal

: C₁₅H₂₆N₂*C₁₁H₂₀LiNO₂

: 110455-86-2
(1Z,3S,4S,5S)-5-Benzyloxy-4-hydroxy-3-methyl-1-hexenyl N,N-diisopropylcarbamate

: 110418-30-9
(1Z,3R,4R,5S)-5-Benzyloxy-4-hydroxy-3-methyl-1-hexenyl N,N-diisopropylcarbamate

Guidance literature:: With titanium(IV) isopropylate; Yield given. Multistep reaction. Yields of byproduct given; 1.) pentane, cyclohexane, isopentane, -70 deg C, 30 min; 2.) pentane, cyclohexane, isopentane, -70 deg C, 4 h;