methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-β-D-mannopyranoside

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Chemical Name:methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-β-D-mannopyranoside
CAS No.:351060-21-4
Molecular Formula:C₅₆H₆₀O₁₂
Molecular Weight:925.085
Hs Code.:

Synonyms:methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-β-D-mannopyranoside

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Chemical Property of methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-β-D-mannopyranoside

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Technology Process of methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-β-D-mannopyranoside

There total 6 articles about methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-β-D-mannopyranoside 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: 81.0%

: 351060-20-3
methyl 2,3,6-tri-O-benzyl-β-D-mannopyranoside

: (2R,4aR,6R,7S,8S,8aR)-6-((R)-Benzenesulfinyl)-7-benzyloxy-8-(4-methoxy-benzyloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine

: 351060-21-4
methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-β-D-mannopyranoside

: methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-α-D-mannopyranosyl)-β-D-mannopyranoside

Guidance literature:: (2R,4aR,6R,7S,8S,8aR)-6-((R)-Benzenesulfinyl)-7-benzyloxy-8-(4-methoxy-benzyloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine; With trifluoromethylsulfonic anhydride; 2,4,6-tri-tert-butylpyrimidine; In dichloromethane; at -78 ℃;

methyl 2,3,6-tri-O-benzyl-β-D-mannopyranoside; In dichloromethane; Further stages.;
DOI:10.1021/ja015985e

Reference yield: 81.0%

: 351060-20-3
methyl 2,3,6-tri-O-benzyl-β-D-mannopyranoside

: phenyl 2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-1-thio-α-D-mannopyranoside S-oxide

: 351060-21-4
methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-β-D-mannopyranoside

: methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-α-D-mannopyranosyl)-β-D-mannopyranoside

Guidance literature:: phenyl 2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-1-thio-α-D-mannopyranoside S-oxide; With 2,4,6-tri-tert-butylpyrimidine; In dichloromethane; at -78 ℃; for 0.5h;

methyl 2,3,6-tri-O-benzyl-β-D-mannopyranoside; With trifluoromethylsulfonic anhydride; In dichloromethane; at -78 ℃; for 1h;
DOI:10.1021/ja0471931

Reference yield:

: 351060-19-0
methyl 2,3-di-O-benzyl-β-D-mannopyranoside

: 351060-21-4
methyl 2,3,6-tri-O-benzyl-4-O-(2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-β-D-mannopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1.1: Bu₂SnO / toluene / 3 h / Heating

1.2: 87 percent / CsF / toluene / 24 h / Heating

2.1: 2,4,6-tri-t-Bu-pyrimidine / CH₂Cl₂ / 0.5 h / -78 °C

2.2: 81 percent / Tf₂O / CH₂Cl₂ / 1 h / -78 °C

With di(n-butyl)tin oxide; 2,4,6-tri-tert-butylpyrimidine; In dichloromethane; toluene;
DOI:10.1021/ja0471931