methyl 4,6-di-O-benzyl-3-O-(2'-O-(p-methoxybenzyl)-4'-O-benzyl-3',6'-dideoxy-α-D-xylo-hexopyranosyl)-α-D-mannopyranoside

Base Information

Chemical Name:methyl 4,6-di-O-benzyl-3-O-(2'-O-(p-methoxybenzyl)-4'-O-benzyl-3',6'-dideoxy-α-D-xylo-hexopyranosyl)-α-D-mannopyranoside
CAS No.:362608-51-3
Molecular Formula:C₄₂H₅₀O₁₀
Molecular Weight:714.853
Hs Code.:

Synonyms:methyl 4,6-di-O-benzyl-3-O-(2'-O-(p-methoxybenzyl)-4'-O-benzyl-3',6'-dideoxy-α-D-xylo-hexopyranosyl)-α-D-mannopyranoside

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Chemical Property of methyl 4,6-di-O-benzyl-3-O-(2'-O-(p-methoxybenzyl)-4'-O-benzyl-3',6'-dideoxy-α-D-xylo-hexopyranosyl)-α-D-mannopyranoside

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Technology Process of methyl 4,6-di-O-benzyl-3-O-(2'-O-(p-methoxybenzyl)-4'-O-benzyl-3',6'-dideoxy-α-D-xylo-hexopyranosyl)-α-D-mannopyranoside

There total 10 articles about methyl 4,6-di-O-benzyl-3-O-(2'-O-(p-methoxybenzyl)-4'-O-benzyl-3',6'-dideoxy-α-D-xylo-hexopyranosyl)-α-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: 94.0%

: 362608-49-9
methyl 2-O-benzoyl-4,6-di-O-benzyl-3-O-(2'-O-(p-methoxybenzyl)-4'-O-benzyl-3',6'-dideoxy-α-D-xylohexopyranosyl)-α-D-mannopyranoside

: 362608-51-3
methyl 4,6-di-O-benzyl-3-O-(2'-O-(p-methoxybenzyl)-4'-O-benzyl-3',6'-dideoxy-α-D-xylo-hexopyranosyl)-α-D-mannopyranoside

Guidance literature:: With sodium methylate; In methanol; at 20 ℃; for 2h;
DOI:10.1560/YXQT-2JJU-YLAA-L04Q

Reference yield:

: 100-39-0
benzyl bromide

: 362608-51-3
methyl 4,6-di-O-benzyl-3-O-(2'-O-(p-methoxybenzyl)-4'-O-benzyl-3',6'-dideoxy-α-D-xylo-hexopyranosyl)-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / sodium hydride / dimethylformamide / 1 h / 20 °C

2: 64 percent / N-iodosuccinimide; silver trifluoromethanesulfonate / CH₂Cl₂ / 0.25 h / 0 °C

3: 94 percent / NaOMe / methanol / 2 h / 20 °C

With N-iodo-succinimide; sodium methylate; silver trifluoromethanesulfonate; sodium hydride; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1560/YXQT-2JJU-YLAA-L04Q

Reference yield:

: 93636-33-0
Benzoic acid (2S,3S,4S,5S,6R)-5-benzyloxy-6-benzyloxymethyl-4-hydroxy-2-methoxy-tetrahydro-pyran-3-yl ester

: 362608-51-3
methyl 4,6-di-O-benzyl-3-O-(2'-O-(p-methoxybenzyl)-4'-O-benzyl-3',6'-dideoxy-α-D-xylo-hexopyranosyl)-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / N-iodosuccinimide; silver trifluoromethanesulfonate / CH₂Cl₂ / 0.25 h / 0 °C

2: 94 percent / NaOMe / methanol / 2 h / 20 °C

With N-iodo-succinimide; sodium methylate; silver trifluoromethanesulfonate; In methanol; dichloromethane;
DOI:10.1560/YXQT-2JJU-YLAA-L04Q