{(E)-3-[(1R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-trimethylsilanyloxy-cyclohex-2-enyl]-allyl}-benzene

Base Information

Chemical Name:{(E)-3-[(1R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-trimethylsilanyloxy-cyclohex-2-enyl]-allyl}-benzene
CAS No.:315221-61-5
Molecular Formula:C₂₄H₄₀O₂Si₂
Molecular Weight:416.751
Hs Code.:

Synonyms:{(E)-3-[(1R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-trimethylsilanyloxy-cyclohex-2-enyl]-allyl}-benzene

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Chemical Property of {(E)-3-[(1R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-trimethylsilanyloxy-cyclohex-2-enyl]-allyl}-benzene

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Technology Process of {(E)-3-[(1R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-trimethylsilanyloxy-cyclohex-2-enyl]-allyl}-benzene

There total 1 articles about {(E)-3-[(1R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-trimethylsilanyloxy-cyclohex-2-enyl]-allyl}-benzene 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:

: 75-77-4
chloro-trimethyl-silane

: 10147-11-2
propargyl benzene

: 164577-42-8
<(4R)-(+)-tert-Butoxydimethylsiloxy>-2-cyclohexen-1-on

: 315221-61-5
{(E)-3-[(1R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-trimethylsilanyloxy-cyclohex-2-enyl]-allyl}-benzene

Guidance literature:: Multistep reaction.;
DOI:10.1002/1521-3765(20000602)6:11<1917::AID-CHEM1917>3.0.CO;2-7

Reference yield:

: 315221-61-5
{(E)-3-[(1R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-trimethylsilanyloxy-cyclohex-2-enyl]-allyl}-benzene

: (Z)-7-[(1R,2R,3R)-3-Hydroxy-6-oxo-2-((E)-3-phenyl-propenyl)-cyclohexyl]-hept-5-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: MeLi / tetrahydrofuran / 0.33 h / -30 °C

1.2: tetrahydrofuran / 0.5 h / -30 °C

2.1: 86 percent / H₂; quinoline / 5percent Pd/BaSO₄ / cyclohexane; benzene / 4 h / 40 °C / 760.05 Torr

3.1: 85 percent / HF; pyridine / acetonitrile

With pyridine; quinoline; hydrogen fluoride; methyllithium; hydrogen; 5percent Pd/BaSO₄; In tetrahydrofuran; cyclohexane; acetonitrile; benzene; 1.1: Metallation / 1.2: Alkylation / 2.1: Catalytic hydrogenation / 3.1: Silyl ether cleavage;
DOI:10.1002/1521-3765(20000602)6:11<1917::AID-CHEM1917>3.0.CO;2-7

Reference yield:

: 315221-61-5
{(E)-3-[(1R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-trimethylsilanyloxy-cyclohex-2-enyl]-allyl}-benzene

: 315221-09-1
(Z)-7-[(1R,2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-6-oxo-2-((E)-3-phenyl-propenyl)-cyclohexyl]-hept-5-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: MeLi / tetrahydrofuran / 0.33 h / -30 °C

1.2: tetrahydrofuran / 0.5 h / -30 °C

2.1: 86 percent / H₂; quinoline / 5percent Pd/BaSO₄ / cyclohexane; benzene / 4 h / 40 °C / 760.05 Torr

With quinoline; methyllithium; hydrogen; 5percent Pd/BaSO₄; In tetrahydrofuran; cyclohexane; benzene; 1.1: Metallation / 1.2: Alkylation / 2.1: Catalytic hydrogenation;
DOI:10.1002/1521-3765(20000602)6:11<1917::AID-CHEM1917>3.0.CO;2-7