(1S,2R,4R)-2-((E)-(R)-1-Allyloxy-3-methyl-hept-2-enyl)-1-isopropyl-4-methyl-cyclohexane

Base Information

Chemical Name:(1S,2R,4R)-2-((E)-(R)-1-Allyloxy-3-methyl-hept-2-enyl)-1-isopropyl-4-methyl-cyclohexane
CAS No.:795278-41-0
Molecular Formula:C₂₁H₃₈O
Molecular Weight:306.532
Hs Code.:

Synonyms:(1S,2R,4R)-2-((E)-(R)-1-Allyloxy-3-methyl-hept-2-enyl)-1-isopropyl-4-methyl-cyclohexane

Suppliers and Price of (1S,2R,4R)-2-((E)-(R)-1-Allyloxy-3-methyl-hept-2-enyl)-1-isopropyl-4-methyl-cyclohexane

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (1S,2R,4R)-2-((E)-(R)-1-Allyloxy-3-methyl-hept-2-enyl)-1-isopropyl-4-methyl-cyclohexane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1S,2R,4R)-2-((E)-(R)-1-Allyloxy-3-methyl-hept-2-enyl)-1-isopropyl-4-methyl-cyclohexane

There total 2 articles about (1S,2R,4R)-2-((E)-(R)-1-Allyloxy-3-methyl-hept-2-enyl)-1-isopropyl-4-methyl-cyclohexane 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: 77.0%

: 106-95-6
allyl bromide

: 289909-79-1
(E)-(R)-1-((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyl)-3-methyl-hept-2-en-1-ol

: 795278-41-0
(1S,2R,4R)-2-((E)-(R)-1-Allyloxy-3-methyl-hept-2-enyl)-1-isopropyl-4-methyl-cyclohexane

Guidance literature:: (E)-(R)-1-((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyl)-3-methyl-hept-2-en-1-ol; With sodium hydride; sodium iodide; In 1,2-dimethoxyethane;

allyl bromide; In 1,2-dimethoxyethane; at 20 ℃; for 48h;
DOI:10.1021/ja046084j

Reference yield:

: 795278-71-6
(E)-1-((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyl)-3-methyl-hept-2-en-1-one

: 795278-41-0
(1S,2R,4R)-2-((E)-(R)-1-Allyloxy-3-methyl-hept-2-enyl)-1-isopropyl-4-methyl-cyclohexane

Guidance literature:: Multi-step reaction with 2 steps

1.1: 82 percent / Et₃BHLi / tetrahydrofuran / 0.08 h / -78 °C

2.1: NaH; sodium iodide / 1,2-dimethoxy-ethane

2.2: 77 percent / 1,2-dimethoxy-ethane / 48 h / 20 °C

With sodium hydride; lithium triethylborohydride; sodium iodide; In tetrahydrofuran; 1,2-dimethoxyethane;
DOI:10.1021/ja046084j

Reference yield:

: 795278-41-0
(1S,2R,4R)-2-((E)-(R)-1-Allyloxy-3-methyl-hept-2-enyl)-1-isopropyl-4-methyl-cyclohexane

: (S)-4-[(E)-2-((1S,2S,5R)-2-Isopropyl-5-methyl-cyclohexyl)-vinyl]-4-methyl-oct-1-en-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / n-BuLi / tetrahydrofuran; hexane / -85 - 20 °C

2: 98 percent / Dess-Martin periodinane / CH₂Cl₂ / 0.33 h / 20 °C

With n-butyllithium; Dess-Martin periodane; In tetrahydrofuran; hexane; dichloromethane; 1: <2,3>-Wittig rearrangement;
DOI:10.1021/ja046084j