Methanesulfonic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-pyran-3-yl ester

Base Information

• Chemical Name: Methanesulfonic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-pyran-3-yl ester
• CAS No.: 797010-94-7
• Molecular Formula: C₃₇H₅₂O₈SSi
• Molecular Weight: 684.967
• Mol file: 797010-94-7.mol

Synonyms:Methanesulfonic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-pyran-3-yl ester

Chemical Property of Methanesulfonic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-pyran-3-yl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of Methanesulfonic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-pyran-3-yl ester

There total 4 articles about Methanesulfonic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-pyran-3-yl 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:

tert-butyldimethylsilyl chloride (18162-48-6) → Methanesulfonic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-pyran-3-yl ester (797010-94-7)

Guidance literature:

Multi-step reaction with 2 steps

1: imidazole / dimethylformamide / 6 h / 20 °C

2: pyridine / 12 h / 20 °C

With pyridine; 1H-imidazole; In N,N-dimethyl-formamide;

DOI:10.1016/j.tetlet.2004.09.030

Reference yield:

3-(3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-1-propene (161275-25-8) → Methanesulfonic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-pyran-3-yl ester (797010-94-7)

Guidance literature:

Multi-step reaction with 3 steps

1.1: BH₃*THF / tetrahydrofuran / 2 h / 0 °C

1.2: 63 percent / H₂O₂; aq. NaOH / tetrahydrofuran / 0.5 h / 20 °C

2.1: imidazole / dimethylformamide / 6 h / 20 °C

3.1: pyridine / 12 h / 20 °C

With pyridine; 1H-imidazole; borane-THF; In tetrahydrofuran; N,N-dimethyl-formamide;

DOI:10.1016/j.tetlet.2004.09.030

Reference yield:

3-C-(3,4,6-tri-O-benzyl-β-D-glucopyranosyl)1-propanol (288584-96-3) → Methanesulfonic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-pyran-3-yl ester (797010-94-7)

Guidance literature:

Multi-step reaction with 2 steps

1: imidazole / dimethylformamide / 6 h / 20 °C

2: pyridine / 12 h / 20 °C

With pyridine; 1H-imidazole; In N,N-dimethyl-formamide;

DOI:10.1016/j.tetlet.2004.09.030

upstream raw materials:

methanesulfonyl chloride

tert-butyldimethylsilyl chloride

3-(3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-1-propene

3-C-(3,4,6-tri-O-benzyl-β-D-glucopyranosyl)1-propanol

Downstream raw materials:

(2R,3R,4R,4aR,8aS)-3,4-Bis-benzyloxy-2-benzyloxymethyl-octahydro-pyrano[3,2-b]pyran

(2R,3R,4R,4aR,8aS)-3-(benzyloxy)-2-(phenoxymethyl)octahydropyrano[3,2-b]pyran-4-ol

Methanesulfonic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-(3-hydroxy-propyl)-tetrahydro-pyran-3-yl ester