ethyl (3R,4S,5S)-4,5-dihydroxy-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate

Base Information

Chemical Name:ethyl (3R,4S,5S)-4,5-dihydroxy-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate
CAS No.:1201685-71-3
Molecular Formula:C₁₄H₂₄O₅
Molecular Weight:272.342
Hs Code.:

Synonyms:ethyl (3R,4S,5S)-4,5-dihydroxy-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate

Suppliers and Price of ethyl (3R,4S,5S)-4,5-dihydroxy-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 2 raw suppliers

Chemical Property of ethyl (3R,4S,5S)-4,5-dihydroxy-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate

Chemical Property:

Purity/Quality:: 95% ^*data from raw suppliers

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Technology Process of ethyl (3R,4S,5S)-4,5-dihydroxy-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate

There total 1 articles about ethyl (3R,4S,5S)-4,5-dihydroxy-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate 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: 67.0%

: 1201685-54-2
ethyl (3aR,7S,7aS)-2,2-diethyl-7-hydroxy-3a,6,7,7a-tetrahydrobenzo[d][1,3]dioxole-5-carboxylate

: 1201685-71-3
ethyl (3R,4S,5S)-4,5-dihydroxy-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate

: C₁₄H₂₄O₅

Guidance literature:: ethyl (3aR,7S,7aS)-2,2-diethyl-7-hydroxy-3a,6,7,7a-tetrahydrobenzo[d][1,3]dioxole-5-carboxylate; With aluminum (III) chloride; In chloroform; at 0 ℃; for 0.05h; Inert atmosphere; Sonication;

With triethylsilane; In chloroform; at -50 - 0 ℃; for 20h; Inert atmosphere;

With water; sodium hydrogencarbonate; In chloroform; regioselective reaction; Inert atmosphere;
DOI:10.1021/ol9024716