{(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile

Base Information

Chemical Name:{(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile
CAS No.:849122-71-0
Molecular Formula:C₂₀H₃₃NO₂
Molecular Weight:319.488
Hs Code.:

Synonyms:{(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile

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Chemical Property of {(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile

Chemical Property:

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Technology Process of {(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile

There total 6 articles about {(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile 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: 91.0%

: 849122-70-9
methanesulfonic acid {(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-methyl ester

: 151-50-8
potassium cyanide

: 849122-71-0
{(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile

Guidance literature:: With 18-crown-6 ether; In acetonitrile; at 80 ℃; for 8h;
DOI:10.1016/j.tet.2004.12.039

Reference yield:

: (1R,2R,6R)-6-Isopropyl-2-((2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl)-3-methyl-cyclohex-3-enecarbaldehyde

: 849122-71-0
{(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 505 mg / NaBH₄ / ethanol / 0.33 h / 20 °C

2: 100 percent / Et₃N / CH₂Cl₂ / 15 h / 20 °C

3: 91 percent / 18-crown-6 / acetonitrile / 8 h / 80 °C

With sodium tetrahydroborate; 18-crown-6 ether; triethylamine; In ethanol; dichloromethane; acetonitrile;
DOI:10.1016/j.tet.2004.12.039

Reference yield:

: 849122-67-4
(2S,3R)-1-[(1R,5R,6R)-6-dimethoxymethyl-5-isopropyl-2-methyl-cyclohex-2-enyl]-3-methyl-pent-4-en-2-ol

: 849122-71-0
{(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-methyl-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile

Guidance literature:: Multi-step reaction with 5 steps

1: 82 percent / DIPEA; TBAI / CH₂Cl₂ / 15 h / 20 °C

2: LiBF₄ / acetonitrile; H₂O / 1 h / 20 °C

3: 505 mg / NaBH₄ / ethanol / 0.33 h / 20 °C

4: 100 percent / Et₃N / CH₂Cl₂ / 15 h / 20 °C

5: 91 percent / 18-crown-6 / acetonitrile / 8 h / 80 °C

With sodium tetrahydroborate; lithium tetrafluoroborate; 18-crown-6 ether; tetra-(n-butyl)ammonium iodide; triethylamine; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane; water; acetonitrile;
DOI:10.1016/j.tet.2004.12.039