p-methoxybenzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1-> 3)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

Base Information

Chemical Name:p-methoxybenzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1-> 3)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside
CAS No.:204982-98-9
Molecular Formula:C₅₆H₅₅NO₁₂
Molecular Weight:934.052
Hs Code.:

Synonyms:p-methoxybenzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1-> 3)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

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Chemical Property of p-methoxybenzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1-> 3)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

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Technology Process of p-methoxybenzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1-> 3)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

There total 3 articles about p-methoxybenzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1-> 3)-4,6-O-benzylidene-2-deoxy-2-phthalimido-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: 97.0%

: 33639-77-9
perbenzyl fucosyl bromide

: 204982-97-8
p-methoxybenzyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

: 204982-98-9
p-methoxybenzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1-> 3)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: With tetrabutylammomium bromide; diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 4h;
DOI:10.1080/07328300008544072

Reference yield:

: 1125-88-8
benzaldehyde dimethyl acetal

: 204982-98-9
p-methoxybenzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1-> 3)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / TsOH / acetonitrile / 0.5 h / 20 °C

2: 97 percent / tetrabutylammonium bromide; diisopropylamine / CH₂Cl₂; dimethylformamide / 4 h / 20 °C

With tetrabutylammomium bromide; toluene-4-sulfonic acid; diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1: acetal formation / 2: Substitution;
DOI:10.1080/07328300008544072

Reference yield:

: 93417-35-7
p-methoxybenzyl 2-deoxy-2-phthalimido-β-D-glucopyranoside

: 204982-98-9
p-methoxybenzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1-> 3)-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / TsOH / acetonitrile / 0.5 h / 20 °C

2: 97 percent / tetrabutylammonium bromide; diisopropylamine / CH₂Cl₂; dimethylformamide / 4 h / 20 °C

With tetrabutylammomium bromide; toluene-4-sulfonic acid; diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1: acetal formation / 2: Substitution;
DOI:10.1080/07328300008544072