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

Base Information

Chemical Name:{(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-(4-methoxyphenoxy)-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile
CAS No.:849122-83-4
Molecular Formula:C₂₆H₃₇NO₄
Molecular Weight:427.584
Hs Code.:

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

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

There total 7 articles about {(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-(4-methoxyphenoxy)-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: 100.0%

: 849122-82-3
methanesulfonic acid (1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-(4-methoxyphenoxy)-pent-4-enyl]-3-methyl-cyclohex-3-enylmethyl ester

: 151-50-8
potassium cyanide

: 849122-83-4
{(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-(4-methoxyphenoxy)-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile

Guidance literature:: With 18-crown-6 ether; In acetonitrile; at 80 ℃; for 2.5h;
DOI:10.1016/j.tet.2004.12.039

Reference yield:

: 848760-88-3
(2S,3R)-1-[(1R,5R,6R)-6-dimethoxymethyl-5-isopropyl-2-methyl-cyclohex-2-enyl]3-(4-methoxyphenoxy)-pent-4-en-2-ol

: 849122-83-4
{(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-(4-methoxyphenoxy)-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile

Guidance literature:: Multi-step reaction with 5 steps

1: 95 percent / DIPEA; TBAI / CH₂Cl₂ / 25 °C

2: aq. LiBF₄ / acetonitrile / 25 °C

3: NaBH₄ / ethanol / 25 °C

4: 95 percent / TEA / CH₂Cl₂ / 0 - 25 °C

5: 100 percent / [18]crown-6 / acetonitrile / 80 °C

With sodium tetrahydroborate; lithium tetrafluoroborate; 18-crown-6 ether; TEA; tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane; acetonitrile;
DOI:10.1002/chem.200500749

Reference yield:

: 849122-81-2
(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-(4-methoxyphenoxy)-pent-4-enyl]-3-methyl-cyclohex-3-enecarbaldehyde

: 849122-83-4
{(1R,2R,6R)-6-isopropyl-2-[(2S,3R)-2-methoxymethoxy-3-(4-methoxyphenoxy)-pent-4-enyl]-3-methyl-cyclohex-3-enyl}-acetonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: NaBH₄ / ethanol / 25 °C

2: 95 percent / TEA / CH₂Cl₂ / 0 - 25 °C

3: 100 percent / [18]crown-6 / acetonitrile / 80 °C

With sodium tetrahydroborate; 18-crown-6 ether; TEA; In ethanol; dichloromethane; acetonitrile;
DOI:10.1002/chem.200500749