Benzyl O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-6-O-benzoyl-2-O-benzyl-β-D-glucopyranoside

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Chemical Name:Benzyl O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-6-O-benzoyl-2-O-benzyl-β-D-glucopyranoside
CAS No.:99322-20-0
Molecular Formula:C₄₇H₄₈O₁₂
Molecular Weight:804.891
Hs Code.:

Synonyms:Benzyl O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-6-O-benzoyl-2-O-benzyl-β-D-glucopyranoside

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Chemical Property of Benzyl O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-6-O-benzoyl-2-O-benzyl-β-D-glucopyranoside

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Technology Process of Benzyl O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-6-O-benzoyl-2-O-benzyl-β-D-glucopyranoside

There total 3 articles about Benzyl O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-6-O-benzoyl-2-O-benzyl-β-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: 91.0%

: 10364-94-0
1-benzoylimidazole

: 99322-18-6
Benzyl O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-2-O-benzyl-β-D-glucopyranoside

: 99322-20-0
Benzyl O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-6-O-benzoyl-2-O-benzyl-β-D-glucopyranoside

Guidance literature:: In chloroform; for 5h; Heating;
DOI:10.1016/S0008-6215(00)90765-1

Reference yield:

: 62867-72-5
benzyl 2,3-di-O-acetyl-4,6-O-benzylidene-β-D-galactopyranosyl-(1→4)-2,3-di-O-acetyl-β-D-glucopyranoside

: 99322-20-0
Benzyl O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-6-O-benzoyl-2-O-benzyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) dibutyltin oxide, 2.) tetrabutylammonium bromide / 1.) benzene, reflux, 5 h, 2.) benzene, 100 deg C, 20 h

2: 91 percent / CHCl₃ / 5 h / Heating

With tetrabutylammomium bromide; di(n-butyl)tin oxide; In chloroform;
DOI:10.1016/S0008-6215(00)90765-1

Reference yield:

: 100-39-0
benzyl bromide

: 99322-20-0
Benzyl O-(3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-(1->4)-6-O-benzoyl-2-O-benzyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) dibutyltin oxide, 2.) tetrabutylammonium bromide / 1.) benzene, reflux, 5 h, 2.) benzene, 100 deg C, 20 h

2: 91 percent / CHCl₃ / 5 h / Heating

With tetrabutylammomium bromide; di(n-butyl)tin oxide; In chloroform;
DOI:10.1016/S0008-6215(00)90765-1