(1S,2S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-isopropenyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-ol

Base Information

Chemical Name:(1S,2S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-isopropenyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-ol
CAS No.:138366-21-9
Molecular Formula:C₂₇H₄₄O₃Si
Molecular Weight:444.73
Hs Code.:

Synonyms:(1S,2S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-isopropenyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-ol

Suppliers and Price of (1S,2S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-isopropenyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-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 (1S,2S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-isopropenyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-ol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1S,2S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-isopropenyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-ol

There total 8 articles about (1S,2S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-isopropenyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-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: 77.0%

: 13291-18-4
isopropenylmagnesium bromide

: 138366-20-8
(1S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-5,6-dimethyl-bicyclo[3.2.1]octan-2-one

: 138366-21-9
(1S,2S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-isopropenyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-ol

Guidance literature:: In tetrahydrofuran; at -78 - 0 ℃;
DOI:10.1016/S0040-4039(00)93591-3

Reference yield:

: (1R,5R,6R,7R,8S)-8-Benzyloxy-7-hydroxymethyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-ol

: 138366-21-9
(1S,2S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-isopropenyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / imidazole / dimethylformamide / 24 °C

2: 75 percent / Swern oxidation

3: 77 percent / tetrahydrofuran / -78 - 0 °C

With 1H-imidazole; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(00)93591-3

Reference yield:

: 138366-16-2,138457-05-3
2-Methoxymethoxy-5,8-dimethyl-6-oxo-tricyclo[3.2.1.0^2,7]octane-1-carboxylic acid ethyl ester

: 138366-21-9
(1S,2S,5R,6R,7R,8S)-8-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-isopropenyl-5,6-dimethyl-bicyclo[3.2.1]octan-2-ol

Guidance literature:: Multi-step reaction with 8 steps

1: NaBH₄ / methanol / 0 °C

2: 94 percent / NaH / tetrahydrofuran; dimethylformamide / 25 °C

3: 91 percent / 36percent HCl / ethanol / 25 °C

4: 99 percent / K₂CO₃ / ethanol

5: 88 percent / LiAlH₄ / diethyl ether / 0 °C

6: 95 percent / imidazole / dimethylformamide / 24 °C

7: 75 percent / Swern oxidation

8: 77 percent / tetrahydrofuran / -78 - 0 °C

With 1H-imidazole; hydrogenchloride; sodium tetrahydroborate; lithium aluminium tetrahydride; sodium hydride; potassium carbonate; In tetrahydrofuran; methanol; diethyl ether; ethanol; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(00)93591-3