(E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-en-1-ol

Base Information

Chemical Name:(E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-en-1-ol
CAS No.:258846-63-8
Molecular Formula:C₂₀H₃₄O₃Si
Molecular Weight:350.574
Hs Code.:

Synonyms:(E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-en-1-ol

Suppliers and Price of (E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-en-1-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 (E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-en-1-ol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-en-1-ol

There total 6 articles about (E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-en-1-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: 95.0%

: (E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-enoic acid

: 258846-63-8
(E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-en-1-ol

Guidance literature:: With diisobutylaluminium hydride; In diethyl ether; at -78 ℃;
DOI:10.1039/a907922j

Reference yield:

: 3587-60-8
Benzyloxymethyl chloride

: 258846-63-8
(E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-en-1-ol

Guidance literature:: Multi-step reaction with 6 steps

1: 70 percent / HMPA; LDA / -78 °C

2: 90 percent / imidazole / dimethylformamide

3: 86 percent / DIBAL-H / diethyl ether / -78 °C

4: (COCl)2; Et₃N; DMSO / CH₂Cl₂ / -65 - -55 °C

5: LiCl; i-Pr₂NEt / acetonitrile

6: 95 percent / DIBAL-H / diethyl ether / -78 °C

With 1H-imidazole; N,N,N,N,N,N-hexamethylphosphoric triamide; oxalyl dichloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; lithium chloride; lithium diisopropyl amide; In diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1: Alkylation / 2: Substitution / 3: Reduction / 4: Oxidation / 5: Condensation / 6: Reduction;
DOI:10.1039/a907922j

Reference yield:

: 107441-54-3
(2R,3R)-methyl 2-[(benzyloxy)methyl]-3-hydroxybutyrate

: 258846-63-8
(E)-(4R,5R)-4-Benzyloxymethyl-5-(tert-butyl-dimethyl-silanyloxy)-hex-2-en-1-ol

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / imidazole / dimethylformamide

2: 86 percent / DIBAL-H / diethyl ether / -78 °C

3: (COCl)2; Et₃N; DMSO / CH₂Cl₂ / -65 - -55 °C

4: LiCl; i-Pr₂NEt / acetonitrile

5: 95 percent / DIBAL-H / diethyl ether / -78 °C

With 1H-imidazole; oxalyl dichloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine; lithium chloride; In diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1: Substitution / 2: Reduction / 3: Oxidation / 4: Condensation / 5: Reduction;
DOI:10.1039/a907922j