(4R,5R)-5-Benzenesulfonylmethyl-1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-heptan-4-ol

Base Information

• Chemical Name: (4R,5R)-5-Benzenesulfonylmethyl-1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-heptan-4-ol
• CAS No.: 503443-79-6
• Molecular Formula: C₃₁H₄₂O₄SSi
• Molecular Weight: 538.824
• Mol file: 503443-79-6.mol

Synonyms:(4R,5R)-5-Benzenesulfonylmethyl-1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-heptan-4-ol

Chemical Property of (4R,5R)-5-Benzenesulfonylmethyl-1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-heptan-4-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (4R,5R)-5-Benzenesulfonylmethyl-1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-heptan-4-ol

There total 6 articles about (4R,5R)-5-Benzenesulfonylmethyl-1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-heptan-4-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: 92.0%

tert-butylchlorodiphenylsilane (58479-61-1) + (4R,5R)-5-Benzenesulfonylmethyl-6-methyl-heptane-1,4-diol (503443-91-2) → (4R,5R)-5-Benzenesulfonylmethyl-1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-heptan-4-ol (503443-79-6)

Guidance literature:

With dmap; triethylamine; In dichloromethane;

DOI:10.1016/S0040-4039(02)02608-4

Reference yield:

(2E)-6-(benzyloxy)hex-2-en-1-ol (83458-91-7) → (4R,5R)-5-Benzenesulfonylmethyl-1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-heptan-4-ol (503443-79-6)

Guidance literature:

Multi-step reaction with 6 steps

1.1: 90 percent / D-(-)-DIPT; Ti(O-i-Pr)4; TBHP / -20 °C

2.1: CuI / tetrahydrofuran / 1.5 h / -50 °C

2.2: 1 h / -78 °C

3.1: 80 percent / Bu₃P / pyridine

4.1: 75 percent / mCPBA / CH₂Cl₂

5.1: 97 percent / Pd/C / methanol

6.1: 92 percent / NEt₃; DMAP / CH₂Cl₂

With titanium(IV) isopropylate; tert.-butylhydroperoxide; dmap; palladium on activated charcoal; copper(l) iodide; tributylphosphine; D-(-)-diisopropyl tartrate; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; pyridine; methanol; dichloromethane; 1.1: Sharpless asymmetric epoxidation;

DOI:10.1016/S0040-4039(02)02608-4

Reference yield:

((2R,3R)-3-(3-(benzyloxy)propyl)oxiran-2-yl)methanol (83458-92-8) → (4R,5R)-5-Benzenesulfonylmethyl-1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-heptan-4-ol (503443-79-6)

Guidance literature:

Multi-step reaction with 5 steps

1.1: CuI / tetrahydrofuran / 1.5 h / -50 °C

1.2: 1 h / -78 °C

2.1: 80 percent / Bu₃P / pyridine

3.1: 75 percent / mCPBA / CH₂Cl₂

4.1: 97 percent / Pd/C / methanol

5.1: 92 percent / NEt₃; DMAP / CH₂Cl₂

With dmap; palladium on activated charcoal; copper(l) iodide; tributylphosphine; triethylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; pyridine; methanol; dichloromethane;

DOI:10.1016/S0040-4039(02)02608-4

upstream raw materials:

tert-butylchlorodiphenylsilane

(4R,5R)-5-Benzenesulfonylmethyl-6-methyl-heptane-1,4-diol

(2E)-6-(benzyloxy)hex-2-en-1-ol

((2R,3R)-3-(3-(benzyloxy)propyl)oxiran-2-yl)methanol

Downstream raw materials:

((4R,5R)-5-Benzenesulfonylmethyl-4-benzyloxy-6-methyl-heptyloxy)-tert-butyl-diphenyl-silane

tert-Butyl-{3-[(2R,3R,5S)-5-((1S,5R)-8,8-dimethoxy-1,5-dimethyl-octyl)-3-isopropyl-tetrahydro-furan-2-yl]-propoxy}-diphenyl-silane

(4R,5R,8S,12R)-4-Benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-5-isopropyl-15,15-dimethoxy-8,12-dimethyl-pentadecan-7-one

(4R,5R,7S,8S,12R)-4-Benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-5-isopropyl-15,15-dimethoxy-8,12-dimethyl-pentadecan-7-ol