methyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

Base Information

• Chemical Name: methyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside
• CAS No.: 164664-85-1
• Molecular Formula: C₇₇H₈₂O₁₇
• Molecular Weight: 1279.49

Synonyms:methyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

Chemical Property of methyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

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Technology Process of methyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

There total 1 articles about methyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-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:

6-O-acetyl-2,3,4-tri-O-benzyl-α,β-D-glucopyranosyl chloride + methyl O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside (164664-76-0) → methyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside (164664-85-1)

Guidance literature:

With 4 A molecular sieve; silver trifluoromethanesulfonate; silver carbonate; Yield given. Multistep reaction; 1.) CH₂Cl₂, -25 deg C, 30 min, 2.) CH₂Cl₂, 8 h;

DOI:10.1016/0008-6215(94)00314-6

Reference yield: 95.0%

methyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside (164664-85-1) → methyl O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

Guidance literature:

With sodium methylate; In methanol; toluene; for 96h; Ambient temperature;

DOI:10.1016/0008-6215(94)00314-6

Reference yield: 93.0%

methyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside (164664-85-1) → methyl O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

Guidance literature:

With sodium methylate; In methanol; toluene; for 3h; Ambient temperature;

DOI:10.1016/0008-6215(94)00315-7

upstream raw materials:

methyl O-(3-O-benzoyl-4-O-benzyl-2-deoxy-α-D-arabino-hexopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

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