((2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-3,6-dimethoxy-tetrahydro-pyran-2-ylmethoxy)-tert-butyl-diphenyl-silane

Base Information

• Chemical Name: ((2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-3,6-dimethoxy-tetrahydro-pyran-2-ylmethoxy)-tert-butyl-diphenyl-silane
• CAS No.: 186540-01-2
• Molecular Formula: C₃₈H₄₆O₆Si
• Molecular Weight: 626.865
• Mol file: 186540-01-2.mol

Synonyms:((2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-3,6-dimethoxy-tetrahydro-pyran-2-ylmethoxy)-tert-butyl-diphenyl-silane

Chemical Property of ((2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-3,6-dimethoxy-tetrahydro-pyran-2-ylmethoxy)-tert-butyl-diphenyl-silane

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of ((2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-3,6-dimethoxy-tetrahydro-pyran-2-ylmethoxy)-tert-butyl-diphenyl-silane

There total 2 articles about ((2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-3,6-dimethoxy-tetrahydro-pyran-2-ylmethoxy)-tert-butyl-diphenyl-silane 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:

methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside (7177-79-9,13035-24-0,13225-19-9,29600-81-5,33164-02-2,51842-18-3,52526-59-7,78738-75-7,99212-27-8,101312-02-1,107795-23-3,129170-92-9,108739-87-3) → ((2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-3,6-dimethoxy-tetrahydro-pyran-2-ylmethoxy)-tert-butyl-diphenyl-silane (186540-01-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 59 percent / 60percent aq. AcOH / 0.75 h / 80 °C

2: 42 percent / imidazole / tetrahydrofuran / 8 h / 25 °C

3: 1.) NaH / 1.) THF, 0 deg C, 10 min, 2.) THF, 25 deg C, 8 h

With 1H-imidazole; sodium hydride; acetic acid; In tetrahydrofuran;

DOI:10.1016/S0968-0896(96)00178-2

Reference yield:

(2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-6-methoxy-tetrahydro-pyran-3-ol (169396-75-2) + methyl iodide (74-88-4) → ((2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-3,6-dimethoxy-tetrahydro-pyran-2-ylmethoxy)-tert-butyl-diphenyl-silane (186540-01-2)

Guidance literature:

With sodium hydride; Yield given. Multistep reaction; 1.) THF, 0 deg C, 10 min, 2.) THF, 25 deg C, 8 h;

DOI:10.1016/S0968-0896(96)00178-2

Reference yield: 80.0%

((2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-3,6-dimethoxy-tetrahydro-pyran-2-ylmethoxy)-tert-butyl-diphenyl-silane (186540-01-2) → methyl 2,3-di-O-benzyl-4-O-methyl-α-D-mannopyranoside (88110-51-4)

Guidance literature:

With pyridine; hydrogen fluoride; In tetrahydrofuran; at 25 ℃; for 8h;

DOI:10.1016/S0968-0896(96)00178-2

upstream raw materials:

(2R,3R,4S,5S,6S)-4,5-Bis-benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-6-methoxy-tetrahydro-pyran-3-ol

methyl iodide

methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Downstream raw materials:

methyl 2,3-di-O-benzyl-4-O-methyl-α-D-mannopyranoside

methyl 4-O-methyl-α-D-mannopyranoside