methyl 6-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzyl-(6S)-C-methyl-α-D-glucopyranoside

Base Information

Chemical Name:methyl 6-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzyl-(6S)-C-methyl-α-D-glucopyranoside
CAS No.:341497-68-5
Molecular Formula:C₅₈H₆₄O₁₂
Molecular Weight:953.139
Hs Code.:

Synonyms:methyl 6-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzyl-(6S)-C-methyl-α-D-glucopyranoside

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Chemical Property of methyl 6-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzyl-(6S)-C-methyl-α-D-glucopyranoside

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Technology Process of methyl 6-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzyl-(6S)-C-methyl-α-D-glucopyranoside

There total 4 articles about methyl 6-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzyl-(6S)-C-methyl-α-D-glucopyranoside 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: 51.0%

: 35094-58-7
6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl bromide

: 341495-66-7
methyl 2,3,4-tri-O-benzyl-(6S)-C-methyl-α-D-glucopyranoside

: 341497-68-5
methyl 6-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzyl-(6S)-C-methyl-α-D-glucopyranoside

Guidance literature:: With tetraethylammonium bromide; N,N-dimethyl-formamide; In dichloromethane;
DOI:10.1139/v01-005

Reference yield:

: 53008-65-4,641635-63-4
methyl 2,3,4-tri-O-benzyl-D-glucopyranoside

: 341497-68-5
methyl 6-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzyl-(6S)-C-methyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1.1: 70 percent / CrO₃; pyridine / CH₂Cl₂ / 0.17 h / 20 °C

2.1: diethyl ether / 2 h / 20 °C

2.2: 0.612 g / pyridine; 4-dimethylaminopyridine / 20 °C

3.1: 97 percent / NaOH / dioxane; H₂O / 1 h

4.1: 51 percent / tetraethylammonium bromide; N,N-dimethylformamide / CH₂Cl₂

With pyridine; chromium(VI) oxide; sodium hydroxide; tetraethylammonium bromide; N,N-dimethyl-formamide; In 1,4-dioxane; diethyl ether; dichloromethane; water; 2.1: Grignard reaction;
DOI:10.1139/v01-005

Reference yield:

: 83051-88-1
methyl 6-aldehydo-2,3,4-tri-O-benzyl-α-D-glucopyranoside

: 341497-68-5
methyl 6-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-2,3,4-tri-O-benzyl-(6S)-C-methyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1.1: diethyl ether / 2 h / 20 °C

1.2: 0.612 g / pyridine; 4-dimethylaminopyridine / 20 °C

2.1: 97 percent / NaOH / dioxane; H₂O / 1 h

3.1: 51 percent / tetraethylammonium bromide; N,N-dimethylformamide / CH₂Cl₂

With sodium hydroxide; tetraethylammonium bromide; N,N-dimethyl-formamide; In 1,4-dioxane; diethyl ether; dichloromethane; water; 1.1: Grignard reaction;
DOI:10.1139/v01-005