(2R,3R,5S)-5-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-(4-methoxybenzyloxy)-2-methylhept-6-en-3-ol

Base Information

Chemical Name:(2R,3R,5S)-5-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-(4-methoxybenzyloxy)-2-methylhept-6-en-3-ol
CAS No.:423151-65-9
Molecular Formula:C₂₄H₄₂O₄Si
Molecular Weight:422.681
Hs Code.:

Synonyms:(2R,3R,5S)-5-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-(4-methoxybenzyloxy)-2-methylhept-6-en-3-ol

Suppliers and Price of (2R,3R,5S)-5-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-(4-methoxybenzyloxy)-2-methylhept-6-en-3-ol

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 (2R,3R,5S)-5-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-(4-methoxybenzyloxy)-2-methylhept-6-en-3-ol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R,3R,5S)-5-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-(4-methoxybenzyloxy)-2-methylhept-6-en-3-ol

There total 10 articles about (2R,3R,5S)-5-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-(4-methoxybenzyloxy)-2-methylhept-6-en-3-ol 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: 82.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 423151-64-8
(3S,5R,6R)-7-(4-methoxybenzyloxy)-6-methyl-3-vinylheptane-1,5-diol

: 423151-65-9
(2R,3R,5S)-5-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-(4-methoxybenzyloxy)-2-methylhept-6-en-3-ol

Guidance literature:: With 1H-imidazole; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1016/S0040-4039(01)02154-2 DOI:10.1039/b507570j

Reference yield:

: 89238-99-3
O-(4-methoxybenzyl)-trichloroacetimidate

: 423151-65-9
(2R,3R,5S)-5-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-(4-methoxybenzyloxy)-2-methylhept-6-en-3-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 62 percent / camphorsulfonic acid / CH₂Cl₂ / 72 h / 0 °C

2: 99 percent / tetrabutylammonium fluoride / tetrahydrofuran / 2 h / 20 °C

3: 82 percent / imidazole / CH₂Cl₂ / 2 h / 20 °C

With 1H-imidazole; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane;
DOI:10.1039/b507570j

Reference yield:

: 423117-83-3
(2'S,3'R,4R,5S,5'R)-3-{5'-[2''-(tert-butyldiphenylsilanyloxy)-ethyl]-3'-hydroxy-2'-methylhept-6'-enoyl}-4-methyl-5-phenyloxazolidin-2-one

: 423151-65-9
(2R,3R,5S)-5-[2-(tert-butyldimethylsilanyloxy)-ethyl]-1-(4-methoxybenzyloxy)-2-methylhept-6-en-3-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 96 percent / LiBH₄ / methanol; diethyl ether / 2.5 h / 0 - 20 °C

2: 62 percent / camphorsulfonic acid / CH₂Cl₂ / 72 h / 0 °C

3: 99 percent / tetrabutylammonium fluoride / tetrahydrofuran / 2 h / 20 °C

4: 82 percent / imidazole / CH₂Cl₂ / 2 h / 20 °C

With 1H-imidazole; lithium borohydride; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; In tetrahydrofuran; methanol; diethyl ether; dichloromethane;
DOI:10.1039/b507570j