methyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

Base Information

• Chemical Name: methyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside
• CAS No.: 1028832-92-9
• Molecular Formula: C₇₄H₈₀O₁₅
• Molecular Weight: 1209.44

Synonyms:methyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

Chemical Property of methyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

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Technology Process of methyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

There total 1 articles about methyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-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: 95.0%

methyl 4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside (1028832-89-4) + 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl trichloroacetimidate (167013-82-3) → methyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside (1028832-92-9)

Guidance literature:

With trimethylsilyl trifluoromethanesulfonate; In diethyl ether; at -30 ℃; for 3h;

DOI:10.1021/ja801574q

Reference yield: 98.0%

methyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside (1028832-92-9) → methyl 3,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside (1028832-94-1)

Guidance literature:

With methanol; sodium methylate; In dichloromethane; at 20 ℃; for 2h;

DOI:10.1021/ja801574q

upstream raw materials:

methyl 4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl trichloroacetimidate

Downstream raw materials:

methyl 3,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->3)-4-O-benzyl-2-O-(naphthylmethyl)-β-L-rhamnopyranosyl-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

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