Dithiocarbonic acid O-{2-benzyloxy-1-[(4S,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl} ester S-methyl ester

Base Information

• Chemical Name: Dithiocarbonic acid O-{2-benzyloxy-1-[(4S,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl} ester S-methyl ester
• CAS No.: 117174-49-9
• Molecular Formula: C₃₃H₄₂O₅S₂Si
• Molecular Weight: 610.911
• Mol file: 117174-49-9.mol

Synonyms:

Chemical Property of Dithiocarbonic acid O-{2-benzyloxy-1-[(4S,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl} ester S-methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of Dithiocarbonic acid O-{2-benzyloxy-1-[(4S,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl} ester S-methyl ester

There total 6 articles about Dithiocarbonic acid O-{2-benzyloxy-1-[(4S,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl} ester S-methyl ester 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:

2,3-O-isopropylidene-D-ribonic-γ-lactone (30725-00-9) → Dithiocarbonic acid O-{2-benzyloxy-1-[(4S,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl} ester S-methyl ester (117174-49-9)

Guidance literature:

Multi-step reaction with 4 steps

1: NaH, glyme

2: LiAlH₄ / diethyl ether / 0 °C

3: 98 percent / imidazole / dimethylformamide

4: 1.) NaH, imidazole

With 1H-imidazole; lithium aluminium tetrahydride; 1,2-dimethoxyethane; sodium hydride; In diethyl ether; N,N-dimethyl-formamide;

DOI:10.1016/S0040-4039(00)86662-9

Reference yield:

5-O-benzyl-2,3-O-isopropylidene-D-ribono-1,4-lactone (85846-80-6) → Dithiocarbonic acid O-{2-benzyloxy-1-[(4S,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl} ester S-methyl ester (117174-49-9)

Guidance literature:

Multi-step reaction with 3 steps

1: LiAlH₄ / diethyl ether / 0 °C

2: 98 percent / imidazole / dimethylformamide

3: 1.) NaH, imidazole

With 1H-imidazole; lithium aluminium tetrahydride; sodium hydride; In diethyl ether; N,N-dimethyl-formamide;

DOI:10.1016/S0040-4039(00)86662-9

Reference yield:

benzyl bromide (100-39-0) → Dithiocarbonic acid O-{2-benzyloxy-1-[(4S,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl} ester S-methyl ester (117174-49-9)

Guidance literature:

Multi-step reaction with 4 steps

1: NaH, glyme

2: LiAlH₄ / diethyl ether / 0 °C

3: 98 percent / imidazole / dimethylformamide

4: 1.) NaH, imidazole

With 1H-imidazole; lithium aluminium tetrahydride; 1,2-dimethoxyethane; sodium hydride; In diethyl ether; N,N-dimethyl-formamide;

DOI:10.1016/S0040-4039(00)86662-9

upstream raw materials:

carbon disulfide

2-Benzyloxy-1-[(4R,5S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethanol

methyl iodide

2,3-O-isopropylidene-D-ribonic-γ-lactone

Downstream raw materials:

[(4S,5R)-5-(2-Benzyloxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy]-tert-butyl-diphenyl-silane

[(4S,5R)-5-(2-Benzyloxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-methanol

Methanesulfonic acid (2S,3R)-5-benzyloxy-2,3-dihydroxy-pentyl ester

Methanesulfonic acid (4S,5R)-5-(2-benzyloxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester