(2S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-vinyl-tetrahydro-furan-2-ol

Base Information

Chemical Name:(2S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-vinyl-tetrahydro-furan-2-ol
CAS No.:848649-95-6
Molecular Formula:C₂₃H₃₀O₃Si
Molecular Weight:382.575
Hs Code.:

Synonyms:(2S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-vinyl-tetrahydro-furan-2-ol

Suppliers and Price of (2S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-vinyl-tetrahydro-furan-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 (2S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-vinyl-tetrahydro-furan-2-ol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-vinyl-tetrahydro-furan-2-ol

There total 1 articles about (2S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-vinyl-tetrahydro-furan-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:

: 99315-76-1
(5S)-5-(tert-butyldiphenylsiloxymethyl)-2(5H)-furanone

: 848649-95-6
(2S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-vinyl-tetrahydro-furan-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / CuBr*Me₂S / tetrahydrofuran / 1 h / -78 °C

2: 99 percent / DIBAL-H / CH₂Cl₂ / 0.5 h / -78 °C

With copper(I) bromide dimethylsulfide complex; diisobutylaluminium hydride; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmcl.2004.08.003

Reference yield: 99.0%

: 67-56-1
methanol

: 848649-95-6
(2S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-vinyl-tetrahydro-furan-2-ol

: 848649-99-0
tert-Butyl-((2S,3R,5S)-5-methoxy-3-vinyl-tetrahydro-furan-2-ylmethoxy)-diphenyl-silane

Guidance literature:: With hydrogenchloride; at 25 ℃; for 0.25h;
DOI:10.1016/j.bmcl.2004.08.003

Reference yield:

: 848649-95-6
(2S,4R,5S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-4-vinyl-tetrahydro-furan-2-ol

: 792922-42-0
[(2S,3S,5S)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-tetrahydro-furan-3-yl]-((1S,3aS,7aS)-4,4,7a-trimethyl-octahydro-inden-1-yl)-methanone

Guidance literature:: Multi-step reaction with 6 steps

1: 99 percent / HCl / 0.25 h / 25 °C

2: 92 percent / OsO₄; NMO; pyridine / acetone / 12 h / 25 °C

3: 89 percent / Pb(OAc)4 / CH₂Cl₂ / 0.33 h / 25 °C

4: 71 percent / CrCl₂; NiCl₂ / dimethylformamide / 1 h / 25 °C

5: 95 percent / Dess-Martin periodinane / CH₂Cl₂ / 8 h / 25 °C

6: 99 percent / H₂ / Pd/C / methanol / 12 h / 25 °C / 760 Torr

With pyridine; chromium dichloride; lead(IV) acetate; hydrogenchloride; osmium(VIII) oxide; N-methyl-2-indolinone; hydrogen; Dess-Martin periodane; nickel dichloride; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide; acetone; 4: Nozaki coupling;
DOI:10.1016/j.bmcl.2004.08.003