(4S,5S)-4,5-Bis-[(S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolane

Base Information

• Chemical Name: (4S,5S)-4,5-Bis-[(S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolane
• CAS No.: 156487-65-9
• Molecular Formula: C₅₅H₆₆O₆Si₂
• Molecular Weight: 879.296
• Mol file: 156487-65-9.mol

Synonyms:(4S,5S)-4,5-Bis-[(S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolane

Chemical Property of (4S,5S)-4,5-Bis-[(S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolane

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (4S,5S)-4,5-Bis-[(S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolane

There total 3 articles about (4S,5S)-4,5-Bis-[(S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolane 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: 96.0%

tert-butylchlorodiphenylsilane (58479-61-1) + 1,6-di-O-benzyl-3,4-O-methylethylidene-L-iditol (134896-17-6) → (4S,5S)-4,5-Bis-[(S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolane (156487-65-9)

Guidance literature:

With 1H-imidazole; dmap; In N,N-dimethyl-formamide; at 0 - 22 ℃; for 10h;

DOI:10.1016/S0040-4039(00)76674-3

Reference yield:

1,2:5,6-dianhydro-3,4-O-methylethylidene-L-iditol (63699-97-8) → (4S,5S)-4,5-Bis-[(S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolane (156487-65-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 83 percent / NaH / dimethylformamide / 24 h / 0 - 22 °C

2: 96 percent / imidazole, DMAP / dimethylformamide / 10 h / 0 - 22 °C

With 1H-imidazole; dmap; sodium hydride; In N,N-dimethyl-formamide;

DOI:10.1016/S0040-4039(00)76674-3

Reference yield:

benzyl alcohol (100-51-6,185532-71-2) → (4S,5S)-4,5-Bis-[(S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxolane (156487-65-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 83 percent / NaH / dimethylformamide / 24 h / 0 - 22 °C

2: 96 percent / imidazole, DMAP / dimethylformamide / 10 h / 0 - 22 °C

With 1H-imidazole; dmap; sodium hydride; In N,N-dimethyl-formamide;

DOI:10.1016/S0040-4039(00)76674-3

upstream raw materials:

tert-butylchlorodiphenylsilane

1,6-di-O-benzyl-3,4-O-methylethylidene-L-iditol

1,2:5,6-dianhydro-3,4-O-methylethylidene-L-iditol

benzyl alcohol

Downstream raw materials:

3,6-di-O-t-butyldiphenylsilyl-4,5-O-isopropylidene-D-myo-inositol

(S)-2-(tert-Butyl-diphenyl-silanyloxy)-2-{(4S,5S)-5-[(S)-1-(tert-butyl-diphenyl-silanyloxy)-2-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-ethanol