methyl [2,3,4-tri-O-benzyl-6-O-benzoyl-β-D-mannopyranosyl]-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

Base Information

Chemical Name:methyl [2,3,4-tri-O-benzyl-6-O-benzoyl-β-D-mannopyranosyl]-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside
CAS No.:1198618-88-0
Molecular Formula:C₆₂H₆₄O₁₂
Molecular Weight:1001.18
Hs Code.:

Synonyms:methyl [2,3,4-tri-O-benzyl-6-O-benzoyl-β-D-mannopyranosyl]-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

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Chemical Property of methyl [2,3,4-tri-O-benzyl-6-O-benzoyl-β-D-mannopyranosyl]-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

Chemical Property:

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Technology Process of methyl [2,3,4-tri-O-benzyl-6-O-benzoyl-β-D-mannopyranosyl]-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

There total 2 articles about methyl [2,3,4-tri-O-benzyl-6-O-benzoyl-β-D-mannopyranosyl]-(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:

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

: C₃₄H₃₃ClO₆

: 1198618-88-0
methyl [2,3,4-tri-O-benzyl-6-O-benzoyl-β-D-mannopyranosyl]-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

: 1198618-87-9
methyl [2,3,4-tri-O-benzyl-6-O-benzoyl-α-D-mannopyranosyl]-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

Guidance literature:: With N-ethyl-N,N-diisopropylamine; lithium iodide; In chloroform; at 45 ℃; for 18h;
DOI:10.1039/d1sc01300a

Reference yield:

: 2,3,4-tri-O-benzyl-6-O-benzoyl-D-mannopyranose

: 1198618-88-0
methyl [2,3,4-tri-O-benzyl-6-O-benzoyl-β-D-mannopyranosyl]-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

: 1198618-87-9
methyl [2,3,4-tri-O-benzyl-6-O-benzoyl-α-D-mannopyranosyl]-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: Triphenylphosphine oxide; oxalyl dichloride / chloroform / 0.5 h / 20 °C

2: lithium iodide; N-ethyl-N,N-diisopropylamine / chloroform / 18 h / 45 °C

With oxalyl dichloride; N-ethyl-N,N-diisopropylamine; Triphenylphosphine oxide; lithium iodide; In chloroform;
DOI:10.1039/d1sc01300a