allyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-O-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Base Information

Chemical Name:allyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-O-2,3,6-tri-O-benzyl-β-D-glucopyranoside
CAS No.:227601-51-6
Molecular Formula:C₇₇H₈₁NO₂₀
Molecular Weight:1340.48
Hs Code.:

allyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-O-2,3,6-tri-O-benzyl-β-D-glucopyranoside

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Chemical Property of allyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-O-2,3,6-tri-O-benzyl-β-D-glucopyranoside

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Technology Process of allyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-O-2,3,6-tri-O-benzyl-β-D-glucopyranoside

There total 2 articles about allyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-O-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:

: 227601-48-1
allyl-O-<2,4,6-tri-O-benzyl-3-O-(4-methoxybenzyl)-β-D-galactopyranosyl>-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: 227601-51-6
allyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-O-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / 90 percent CF₃COOH / CH₂Cl₂ / 0.25 h / 20 °C

2: 1.) Hg(CN)2, HgBr₂, 4 Angstroem molecular sieves / 1.) CH₃CN, 20 deg C, 2 h, 2.) CH₃CN, 20 deg C, 20 h

With 4 A molecular sieve; mercury(II) cyanide; trifluoroacetic acid; mercury dibromide; In dichloromethane;

Reference yield:

: 70831-94-6
3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-D-glucopyranosyl bromide

: 227601-43-6
allyl-O-<2,4,6-tri-O-benzyl-β-D-galactopyranosyl>-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

: 227601-51-6
allyl-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->3)-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-O-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Guidance literature:: With 4 A molecular sieve; mercury(II) cyanide; mercury dibromide; Yield given; Multistep reaction; 1.) CH₃CN, 20 deg C, 2 h, 2.) CH₃CN, 20 deg C, 20 h;