p-methoxyphenyl O-[2,3-O-(p-methoxybenzylidene)-4,6-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-β-D-mannopyranosyl]-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Base Information

Chemical Name:p-methoxyphenyl O-[2,3-O-(p-methoxybenzylidene)-4,6-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-β-D-mannopyranosyl]-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
CAS No.:309929-66-6
Molecular Formula:C₆₁H₇₅NO₁₅Si₂
Molecular Weight:1118.44
Hs Code.:

p-methoxyphenyl O-[2,3-O-(p-methoxybenzylidene)-4,6-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-β-D-mannopyranosyl]-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Synonyms:p-methoxyphenyl O-[2,3-O-(p-methoxybenzylidene)-4,6-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-β-D-mannopyranosyl]-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

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Chemical Property of p-methoxyphenyl O-[2,3-O-(p-methoxybenzylidene)-4,6-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-β-D-mannopyranosyl]-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

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Technology Process of p-methoxyphenyl O-[2,3-O-(p-methoxybenzylidene)-4,6-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-β-D-mannopyranosyl]-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

There total 1 articles about p-methoxyphenyl O-[2,3-O-(p-methoxybenzylidene)-4,6-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-β-D-mannopyranosyl]-(1-> 4)-3,6-di-O-benzyl-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: 78.0%

: 215722-18-2
p-methoxyphenyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside-methyl 4',6'-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-3'-O-trimethylsilyl-1'-thio-α-D-mannopyranoside-2',4-p-methoxybenzylidene acetal

: 309929-66-6
p-methoxyphenyl O-[2,3-O-(p-methoxybenzylidene)-4,6-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-β-D-mannopyranosyl]-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: p-methoxyphenyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside-methyl 4',6'-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-3'-O-trimethylsilyl-1'-thio-α-D-mannopyranoside-2',4-p-methoxybenzylidene acetal; With 2,6-di-tert-butyl-4-methylpyridine; 4 A molecular sieve; methyl trifluoromethanesulfonate; In 1,2-dichloro-ethane; at 20 ℃; for 0.5h;

at 60 ℃; for 14h;
DOI:10.1016/S0008-6215(00)00123-3

Reference yield: 99.0%

: 309929-66-6
p-methoxyphenyl O-[2,3-O-(p-methoxybenzylidene)-4,6-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-β-D-mannopyranosyl]-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

: 309929-67-7
p-methoxyphenyl 2,3-O-p-methoxybenzylidene-β-D-mannopyranosyl-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 0.75h;
DOI:10.1016/S0008-6215(00)00123-3

Reference yield:

: 309929-66-6
p-methoxyphenyl O-[2,3-O-(p-methoxybenzylidene)-4,6-O-(1,1,3,3-tetraisopropyl)disiloxanylidene-β-D-mannopyranosyl]-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

: 309929-68-8
p-methoxyphenyl 4,6-O-di-tert-butylsilanediyl-β-D-mannopranosyl-(1-> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucpyranoside

Guidance literature:: Multi-step reaction with 2 steps

1.1: 99 percent / tetrabutyl ammonium fluoride / tetrahydrofuran / 0.75 h / 0 °C

2.1: 2,6-di-tert-butyl-4-methylpyridine / dimethylformamide / 1.5 h / 20 °C

2.2: 93 percent / pyridinium p-toluenesulfonate / CH₂Cl₂; methanol / 2.5 h / 20 °C

With 2,6-di-tert-butyl-4-methylpyridine; tetrabutyl ammonium fluoride; In tetrahydrofuran; N,N-dimethyl-formamide; 1.1: Ring cleavage / 2.1: Alkylation / 2.2: Ring cleavage;
DOI:10.1016/S0008-6215(00)00123-3