5-Benzyloxy-1-(tert-butyldiphenylsilanyloxy)-2-methylpentane-3-ol

Base Information

• Chemical Name: 5-Benzyloxy-1-(tert-butyldiphenylsilanyloxy)-2-methylpentane-3-ol
• CAS No.: 301230-09-1
• Molecular Formula: C₂₉H₃₈O₃Si
• Molecular Weight: 462.704
• Mol file: 301230-09-1.mol

Synonyms:5-Benzyloxy-1-(tert-butyldiphenylsilanyloxy)-2-methylpentane-3-ol

Chemical Property of 5-Benzyloxy-1-(tert-butyldiphenylsilanyloxy)-2-methylpentane-3-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-Benzyloxy-1-(tert-butyldiphenylsilanyloxy)-2-methylpentane-3-ol

There total 7 articles about 5-Benzyloxy-1-(tert-butyldiphenylsilanyloxy)-2-methylpentane-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: 94.0%

5-Benzyloxy-2-methylpentane-1,3-diol (105560-79-0) + tert-butylchlorodiphenylsilane (58479-61-1) → 5-Benzyloxy-1-(tert-butyldiphenylsilanyloxy)-2-methylpentane-3-ol (301230-09-1)

Guidance literature:

With 1H-imidazole; In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1039/b000751j

Reference yield:

3-benzyloxypropan-1-ol (4799-68-2) → 5-Benzyloxy-1-(tert-butyldiphenylsilanyloxy)-2-methylpentane-3-ol (301230-09-1)

Guidance literature:

Multi-step reaction with 5 steps

1: 98 percent / oxalyl chloride; methyl sulfoxide; Et₃N / CH₂Cl₂ / -78 - 20 °C

2: 0.543 g / pyridine / CH₂Cl₂

3: 93 percent / 4-dimethylaminopyridine / pyridine / CH₂Cl₂ / 0 - 20 °C

With pyridine; dmap; oxalyl dichloride; dimethyl sulfoxide; triethylamine; pyridine; In dichloromethane; 1: Swern oxidation;

DOI:10.1021/ja0686256

Reference yield:

3-Benzyloxypropanal (19790-60-4) → 5-Benzyloxy-1-(tert-butyldiphenylsilanyloxy)-2-methylpentane-3-ol (301230-09-1)

Guidance literature:

Multi-step reaction with 4 steps

1: 0.543 g / pyridine / CH₂Cl₂

2: 93 percent / 4-dimethylaminopyridine / pyridine / CH₂Cl₂ / 0 - 20 °C

With pyridine; dmap; pyridine; In dichloromethane;

DOI:10.1021/ja0686256

upstream raw materials:

5-Benzyloxy-2-methylpentane-1,3-diol

tert-butylchlorodiphenylsilane

3-benzyloxypropan-1-ol

3-Benzyloxypropanal

Downstream raw materials:

4-Benzyl-3-[(2S,3R,5R,6S)-2-(3-benzyloxy-propyl)-7-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-5-methoxy-6-methyl-heptanoyl]-oxazolidin-2-one

(2R,3R,5R,6S)-2-(3-Benzyloxy-propyl)-7-(tert-butyl-diphenyl-silanyloxy)-5-methoxy-3-methoxymethoxy-6-methyl-heptan-1-ol

(E)-(4R,5R,9S,10R,12R,13S)-16-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxy)-4,10-dimethoxy-12-methoxymethoxy-5,9,13-trimethyl-hexadec-7-en-6-one

(2R,3R,5R,6S)-9-Benzyloxy-3-methoxy-5-methoxymethoxy-2,6-dimethyl-nonanal