allyl O-(2,3,4-tri-O-benzyl-6-O-p-nitrobenzenesulfonyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Base Information

Chemical Name:allyl O-(2,3,4-tri-O-benzyl-6-O-p-nitrobenzenesulfonyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
CAS No.:171412-10-5
Molecular Formula:C₆₃H₆₅NO₁₅S
Molecular Weight:1108.27
Hs Code.:

Synonyms:allyl O-(2,3,4-tri-O-benzyl-6-O-p-nitrobenzenesulfonyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

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Chemical Property of allyl O-(2,3,4-tri-O-benzyl-6-O-p-nitrobenzenesulfonyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

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Technology Process of allyl O-(2,3,4-tri-O-benzyl-6-O-p-nitrobenzenesulfonyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

There total 2 articles about allyl O-(2,3,4-tri-O-benzyl-6-O-p-nitrobenzenesulfonyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-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: 27.0%

: 171411-89-5
allyl O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: 98-74-8
4-Nitrobenzenesulfonyl chloride

: 171412-10-5
allyl O-(2,3,4-tri-O-benzyl-6-O-p-nitrobenzenesulfonyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: allyl O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-benzyl-β-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: 171411-90-8
allyl O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: With N,N-dimethyl acetamide; silver trifluoromethanesulfonate; triethylamine; In dichloromethane; at -40 - 0 ℃;
DOI:10.1246/bcsj.68.2331

Reference yield: 19.0%

: O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-D-glucopyranose

: 171411-89-5
allyl O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: 171412-10-5
allyl O-(2,3,4-tri-O-benzyl-6-O-p-nitrobenzenesulfonyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: allyl O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-benzyl-β-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: 171411-90-8
allyl O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: With N,N-dimethyl acetamide; silver trifluoromethanesulfonate; triethylamine; 4-Nitrobenzenesulfonyl chloride; In dichloromethane; at -40 - 0 ℃;
DOI:10.1246/bcsj.68.2331

Reference yield:

: 171412-10-5
allyl O-(2,3,4-tri-O-benzyl-6-O-p-nitrobenzenesulfonyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: 171411-89-5
allyl O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: dimethylformamide / 3 h / 80 °C

2: MeONa / methanol

With sodium methylate; In methanol; N,N-dimethyl-formamide;
DOI:10.1246/bcsj.68.2331