benzyl O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-(1<*>4)-2,3-di-O-methyl-α-L-rhamnopyranoside

Base Information

Chemical Name:benzyl O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-(1<*>4)-2,3-di-O-methyl-α-L-rhamnopyranoside
CAS No.:89315-96-8
Molecular Formula:C₃₇H₄₈O₁₀
Molecular Weight:652.782
Hs Code.:

Synonyms:benzyl O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-(1<*>4)-2,3-di-O-methyl-α-L-rhamnopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of benzyl O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-(1<*>4)-2,3-di-O-methyl-α-L-rhamnopyranoside

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Technology Process of benzyl O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-(1<*>4)-2,3-di-O-methyl-α-L-rhamnopyranoside

There total 1 articles about benzyl O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-(1<*>4)-2,3-di-O-methyl-α-L-rhamnopyranoside 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: 91.8%

: 89315-95-7
benzyl O-(2,4-di-O-benzyl-3-O-methyl-β-D-glucopyranosyl)-(1<*>4)-α-L-rhamnopyranoside

: 74-88-4
methyl iodide

: 89315-96-8
benzyl O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-(1<*>4)-2,3-di-O-methyl-α-L-rhamnopyranoside

Guidance literature:: With dimethyl sulfoxide; deprotonated form; In dimethyl sulfoxide; at 20 ℃; for 2h;
DOI:10.1016/S0008-6215(00)90396-3

Reference yield: 80.9%

: 89315-96-8
benzyl O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-(1<*>4)-2,3-di-O-methyl-α-L-rhamnopyranoside

: 89821-88-5
O-(3,6-di-O-methyl-β-D-glucopyranosyl)-(1<*>4)-2,3-di-O-methyl-α-L-rhamnopyranoside

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; chloroform; for 16h; Ambient temperature;
DOI:10.1016/S0008-6215(00)90396-3