4-methoxyphenyl 3-O-[D7]benzyl-4,6-di-O-acetyl-α-D-glucopyranosyl-(1->2)-3-O-[D7]benzyl-2,4,6-tri-O-acetyl-β-D-glucopyranoside

Base Information

Chemical Name:4-methoxyphenyl 3-O-[D7]benzyl-4,6-di-O-acetyl-α-D-glucopyranosyl-(1->2)-3-O-[D7]benzyl-2,4,6-tri-O-acetyl-β-D-glucopyranoside
CAS No.:1075708-72-3
Molecular Formula:C₄₃H₅₀O₁₇
Molecular Weight:852.749
Hs Code.:

Synonyms:4-methoxyphenyl 3-O-[D7]benzyl-4,6-di-O-acetyl-α-D-glucopyranosyl-(1->2)-3-O-[D7]benzyl-2,4,6-tri-O-acetyl-β-D-glucopyranoside

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Chemical Property of 4-methoxyphenyl 3-O-[D7]benzyl-4,6-di-O-acetyl-α-D-glucopyranosyl-(1->2)-3-O-[D7]benzyl-2,4,6-tri-O-acetyl-β-D-glucopyranoside

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Technology Process of 4-methoxyphenyl 3-O-[D7]benzyl-4,6-di-O-acetyl-α-D-glucopyranosyl-(1->2)-3-O-[D7]benzyl-2,4,6-tri-O-acetyl-β-D-glucopyranoside

There total 1 articles about 4-methoxyphenyl 3-O-[D7]benzyl-4,6-di-O-acetyl-α-D-glucopyranosyl-(1->2)-3-O-[D7]benzyl-2,4,6-tri-O-acetyl-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: 72.0%

: 1075708-71-2
2-naphthaldehyde (4-methoxyphenyl 3-O-[D7]benzyl-4,6-O-cyclohexylidene-β-D-glucopyranosid-2-yl) (methyl 3-O-[D7]benzyl-4,6-O-cyclohexylidene-1-thio-β-D-glucopyranosid-2-yl) acetal

: 108-24-7
acetic anhydride

: 76-05-1
trifluoroacetic acid

: 1075708-72-3
4-methoxyphenyl 3-O-[D7]benzyl-4,6-di-O-acetyl-α-D-glucopyranosyl-(1->2)-3-O-[D7]benzyl-2,4,6-tri-O-acetyl-β-D-glucopyranoside

Guidance literature:: 2-naphthaldehyde (4-methoxyphenyl 3-O-[D7]benzyl-4,6-O-cyclohexylidene-β-D-glucopyranosid-2-yl) (methyl 3-O-[D7]benzyl-4,6-O-cyclohexylidene-1-thio-β-D-glucopyranosid-2-yl) acetal; With 2,6-di-tert-butyl-4-methylpyridine; methyl trifluoromethanesulfonate; In 1,2-dichloro-ethane; at 20 ℃; for 21h; Molecular sieve; Inert atmosphere;

trifluoroacetic acid; In dichloromethane; at 0 ℃; for 3h;

acetic anhydride; With pyridine; dmap; at 20 ℃; for 12h;
DOI:10.1002/ejoc.200800249