methyl 2,3,6-tri-O-benzoyl-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-α-D-galactopyranosyl)-β-D-galactopyranoside

Base Information

Chemical Name:methyl 2,3,6-tri-O-benzoyl-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-α-D-galactopyranosyl)-β-D-galactopyranoside
CAS No.:96120-70-6
Molecular Formula:C₄₅H₄₃BrO₁₆
Molecular Weight:919.731
Hs Code.:

Synonyms:methyl 2,3,6-tri-O-benzoyl-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-α-D-galactopyranosyl)-β-D-galactopyranoside

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Chemical Property of methyl 2,3,6-tri-O-benzoyl-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-α-D-galactopyranosyl)-β-D-galactopyranoside

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Technology Process of methyl 2,3,6-tri-O-benzoyl-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-α-D-galactopyranosyl)-β-D-galactopyranoside

There total 7 articles about methyl 2,3,6-tri-O-benzoyl-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-α-D-galactopyranosyl)-β-D-galactopyranoside 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: 79.0%

: C₄₅H₄₄O₁₆

: 96120-70-6
methyl 2,3,6-tri-O-benzoyl-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-α-D-galactopyranosyl)-β-D-galactopyranoside

Guidance literature:: With N-Bromosuccinimide; barium carbonate; In tetrachloromethane; for 0.5h; Heating;
DOI:10.1016/0008-6215(85)85169-7

Reference yield:

: 34820-01-4,6344-46-3
methyl 2,3,6-tri-O-benzoyl-β-D-galactopyranoside

: 96120-70-6
methyl 2,3,6-tri-O-benzoyl-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-α-D-galactopyranosyl)-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 11.2 g / silver trifluoromethanesulfonate; 2,4,6-trimethylpyridine / toluene / 2 h / Ambient temperature

2: 80 percent / H₂ / 10 percent Pd/C / acetic acid

3: 91 percent / formic acid / 0.03 h / Ambient temperature

4: pyridine / Ambient temperature

5: 79 percent / N-bromosuccinimide, barium carbonate / CCl₄ / 0.5 h / Heating

With 2,4,6-trimethyl-pyridine; N-Bromosuccinimide; hydrogen; silver trifluoromethanesulfonate; barium carbonate; palladium on activated charcoal; In pyridine; tetrachloromethane; formic acid; acetic acid; toluene;
DOI:10.1016/0008-6215(85)85169-7

Reference yield:

: 4291-68-3,25320-59-6,41110-63-8,67068-83-1,67773-44-8,69237-96-3,92470-93-4,93601-69-5,113829-62-2
(2R,3S,4S,5R,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-chloro-tetrahydro-pyran

: 96120-70-6
methyl 2,3,6-tri-O-benzoyl-4-O-(2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-α-D-galactopyranosyl)-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 11.2 g / silver trifluoromethanesulfonate; 2,4,6-trimethylpyridine / toluene / 2 h / Ambient temperature

2: 80 percent / H₂ / 10 percent Pd/C / acetic acid

3: 91 percent / formic acid / 0.03 h / Ambient temperature

4: pyridine / Ambient temperature

5: 79 percent / N-bromosuccinimide, barium carbonate / CCl₄ / 0.5 h / Heating

With 2,4,6-trimethyl-pyridine; N-Bromosuccinimide; hydrogen; silver trifluoromethanesulfonate; barium carbonate; palladium on activated charcoal; In pyridine; tetrachloromethane; formic acid; acetic acid; toluene;
DOI:10.1016/0008-6215(85)85169-7