(E)-1-[(1R,3R)-3-((E)-4-Hydroxy-3-methyl-but-2-enyl)-2,2-dimethyl-6-methylene-cyclohexyl]-3-methyl-penta-1,4-dien-3-ol

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Chemical Name:(E)-1-[(1R,3R)-3-((E)-4-Hydroxy-3-methyl-but-2-enyl)-2,2-dimethyl-6-methylene-cyclohexyl]-3-methyl-penta-1,4-dien-3-ol
CAS No.:192068-21-6
Molecular Formula:C₂₀H₃₂O₂
Molecular Weight:304.473
Hs Code.:

Synonyms:(E)-1-[(1R,3R)-3-((E)-4-Hydroxy-3-methyl-but-2-enyl)-2,2-dimethyl-6-methylene-cyclohexyl]-3-methyl-penta-1,4-dien-3-ol

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Chemical Property of (E)-1-[(1R,3R)-3-((E)-4-Hydroxy-3-methyl-but-2-enyl)-2,2-dimethyl-6-methylene-cyclohexyl]-3-methyl-penta-1,4-dien-3-ol

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Technology Process of (E)-1-[(1R,3R)-3-((E)-4-Hydroxy-3-methyl-but-2-enyl)-2,2-dimethyl-6-methylene-cyclohexyl]-3-methyl-penta-1,4-dien-3-ol

There total 3 articles about (E)-1-[(1R,3R)-3-((E)-4-Hydroxy-3-methyl-but-2-enyl)-2,2-dimethyl-6-methylene-cyclohexyl]-3-methyl-penta-1,4-dien-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: 60.0%

: 1826-67-1
vinyl magnesium bromide

: 192068-20-5
4-[(1R,3R)-3-(4-hydroxy-3-methylbut-2-enyl)-2,2-dimethyl-6-methylidenecyclohexyl]but-3-en-2-one

: 192068-21-6
(E)-1-[(1R,3R)-3-((E)-4-Hydroxy-3-methyl-but-2-enyl)-2,2-dimethyl-6-methylene-cyclohexyl]-3-methyl-penta-1,4-dien-3-ol

Guidance literature:: In diethyl ether; at -50 ℃; for 0.333333h;
DOI:10.1002/hlca.19970800315

Reference yield:

: 192068-13-6
4-{(1R,3R)-2,2-dimethyl-3-[2-(2-methyl-1,3-dioxolan-2-yl)ethenyl]-4-methylidenecyclohexyl}-2-methylbut-2-en-1-ol

: 192068-21-6
(E)-1-[(1R,3R)-3-((E)-4-Hydroxy-3-methyl-but-2-enyl)-2,2-dimethyl-6-methylene-cyclohexyl]-3-methyl-penta-1,4-dien-3-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / pyridinium toluene-4-sulfonate / acetone; H₂O / 0.5 h / 50 °C

2: 60 percent / diethyl ether / 0.33 h / -50 °C

With pyridinium p-toluenesulfonate; In diethyl ether; water; acetone;
DOI:10.1002/hlca.19970800315

Reference yield:

: (E)-4-{(R)-2,2-Dimethyl-3-[(E)-2-(2-methyl-[1,3]dioxolan-2-yl)-vinyl]-4-methylene-cyclohexyl}-2-methyl-but-2-enoic acid ethyl ester

: 192068-21-6
(E)-1-[(1R,3R)-3-((E)-4-Hydroxy-3-methyl-but-2-enyl)-2,2-dimethyl-6-methylene-cyclohexyl]-3-methyl-penta-1,4-dien-3-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 38.4 percent / DIBAH / hexane / -70 - -65 °C

2: 100 percent / pyridinium toluene-4-sulfonate / acetone; H₂O / 0.5 h / 50 °C

3: 60 percent / diethyl ether / 0.33 h / -50 °C

With pyridinium p-toluenesulfonate; diisobutylaluminium hydride; In diethyl ether; hexane; water; acetone;
DOI:10.1002/hlca.19970800315