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

Base Information

Chemical Name:7-[(1R,2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-6-oxo-2-((E)-3-phenyl-propenyl)-cyclohexyl]-hept-5-ynoic acid methyl ester
CAS No.:315220-98-5
Molecular Formula:C₂₉H₄₂O₄Si
Molecular Weight:482.736
Hs Code.:

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

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Chemical Property of 7-[(1R,2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-6-oxo-2-((E)-3-phenyl-propenyl)-cyclohexyl]-hept-5-ynoic acid methyl ester

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Technology Process of 7-[(1R,2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-6-oxo-2-((E)-3-phenyl-propenyl)-cyclohexyl]-hept-5-ynoic acid methyl ester

There total 3 articles about 7-[(1R,2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-6-oxo-2-((E)-3-phenyl-propenyl)-cyclohexyl]-hept-5-ynoic acid methyl ester 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:

: 149862-39-5
7-Trifluoromethanesulfonyloxy-hept-5-ynoic acid methyl ester

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

: 315220-98-5
7-[(1R,2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-6-oxo-2-((E)-3-phenyl-propenyl)-cyclohexyl]-hept-5-ynoic acid methyl ester

Guidance literature:: {(E)-3-[(1R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-trimethylsilanyloxy-cyclohex-2-enyl]-allyl}-benzene; With methyllithium; In tetrahydrofuran; at -30 ℃; for 0.333333h;

7-Trifluoromethanesulfonyloxy-hept-5-ynoic acid methyl ester; In tetrahydrofuran; at -30 ℃; for 0.5h; Further stages.;
DOI:10.1002/1521-3765(20000602)6:11<1917::AID-CHEM1917>3.0.CO;2-7

Reference yield:

: 50781-91-4
methyl 7-hydroxy-5-heptynoate

: 315220-98-5
7-[(1R,2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-6-oxo-2-((E)-3-phenyl-propenyl)-cyclohexyl]-hept-5-ynoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 2,6-di-tert-butylpyridine / CH₂Cl₂ / 0.25 h / -30 °C

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

2.2: tetrahydrofuran / 0.5 h / -30 °C

With 2,6-di-tert-butyl-pyridine; methyllithium; In tetrahydrofuran; dichloromethane; 1.1: Esterification / 2.1: Metallation / 2.2: Alkylation;
DOI:10.1002/1521-3765(20000602)6:11<1917::AID-CHEM1917>3.0.CO;2-7

Reference yield:

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

: 315220-98-5
7-[(1R,2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-6-oxo-2-((E)-3-phenyl-propenyl)-cyclohexyl]-hept-5-ynoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

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

2.2: tetrahydrofuran / 0.5 h / -30 °C

With methyllithium; In tetrahydrofuran; 2.1: Metallation / 2.2: Alkylation;
DOI:10.1002/1521-3765(20000602)6:11<1917::AID-CHEM1917>3.0.CO;2-7