p-methoxyphenyl (3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranosyluryl)-(1-4)-2-azido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-trifluoroethylsulfonato-β-D-galactopyranoside

Base Information

Chemical Name:p-methoxyphenyl (3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranosyluryl)-(1-4)-2-azido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-trifluoroethylsulfonato-β-D-galactopyranoside
CAS No.:763129-88-0
Molecular Formula:C₅₀H₅₉F₆N₃O₁₈S₂Si
Molecular Weight:1196.24
Hs Code.:

p-methoxyphenyl (3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranosyluryl)-(1-4)-2-azido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-trifluoroethylsulfonato-β-D-galactopyranoside

Synonyms:p-methoxyphenyl (3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranosyluryl)-(1-4)-2-azido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-trifluoroethylsulfonato-β-D-galactopyranoside

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Chemical Property of p-methoxyphenyl (3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranosyluryl)-(1-4)-2-azido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-trifluoroethylsulfonato-β-D-galactopyranoside

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Technology Process of p-methoxyphenyl (3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranosyluryl)-(1-4)-2-azido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-trifluoroethylsulfonato-β-D-galactopyranoside

There total 3 articles about p-methoxyphenyl (3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranosyluryl)-(1-4)-2-azido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-trifluoroethylsulfonato-β-D-galactopyranoside 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: 10.0%

: 640273-65-0
Benzoic acid (2R,3R,4R,5R,6R)-3-azido-6-benzyloxymethyl-2-(2,2,2-trichloro-acetimidoyloxy)-5-(2,2,2-trifluoro-ethoxysulfonyloxy)-tetrahydro-pyran-4-yl ester

: 763129-84-6
p-methoxyphenyl 3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranoside

: 763129-88-0
p-methoxyphenyl (3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranosyluryl)-(1-4)-2-azido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-trifluoroethylsulfonato-β-D-galactopyranoside

Guidance literature:: With boron trifluoride diethyl etherate; In toluene; at 20 ℃; for 8h;
DOI:10.1016/j.tetlet.2004.06.131

Reference yield:

: 303127-81-3
p-methoxyphenyl 3-O-benzyl-4,6-di-O-benzylidene-β-D-glucopyranoside

: 763129-88-0
p-methoxyphenyl (3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranosyluryl)-(1-4)-2-azido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-trifluoroethylsulfonato-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1.1: Me₃N*SO₃ / dimethylformamide; methanol / 48 h / 50 °C

1.2: 86 percent / citric acid / acetonitrile / 48 h / 20 °C

2.1: p-toluenesulfonic acid; ethanethiol / CH₂Cl₂ / 20 °C

2.2: 92 percent / imidazole / dimethylformamide / 1.5 h / 0 °C

3.1: 10 percent / BF₃*OEt₂ / toluene / 8 h / 20 °C

With boron trifluoride diethyl etherate; sulfur trioxide trimethylamine complex; toluene-4-sulfonic acid; ethanethiol; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.tetlet.2004.06.131

Reference yield:

: 763129-80-2
p-methoxypheyl 3-O-benzyl-4,6-O-benzylidene-2-O-trifluoroethylsulfonato-β-D-glucopyranoside

: 763129-88-0
p-methoxyphenyl (3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-trifluoroethylsulfonato-β-D-glucopyranosyluryl)-(1-4)-2-azido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-trifluoroethylsulfonato-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1.1: p-toluenesulfonic acid; ethanethiol / CH₂Cl₂ / 20 °C

1.2: 92 percent / imidazole / dimethylformamide / 1.5 h / 0 °C

2.1: 10 percent / BF₃*OEt₂ / toluene / 8 h / 20 °C

With boron trifluoride diethyl etherate; toluene-4-sulfonic acid; ethanethiol; In dichloromethane; toluene;
DOI:10.1016/j.tetlet.2004.06.131