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

Base Information

• Chemical Name: methyl (2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-2-O-benzyl-α-D-glucopyranoside
• CAS No.: 1220097-83-5
• Molecular Formula: C₄₁H₄₈O₁₀
• Molecular Weight: 700.826
• Mol file: 1220097-83-5.mol

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

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

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

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

There total 3 articles about methyl (2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-2-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: 79.0%

methyl (2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside (1220286-27-0) → methyl (2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-2-O-benzyl-α-D-glucopyranoside (1220097-83-5)

Guidance literature:

With HClO₄-SiO₂; In water; acetonitrile; at 20 ℃; for 0.333333h;

DOI:10.1080/07328300903477804

Reference yield:

methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside (76375-66-1) → methyl (2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-2-O-benzyl-α-D-glucopyranoside (1220097-83-5)

Guidance literature:

Multi-step reaction with 3 steps

1: N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate / dichloromethane / 1 h / -40 °C / Inert atmosphere; Molecular sieve

2: tetrabutylammomium bromide; sodium hydroxide / tetrahydrofuran / 6 h / 20 °C

3: HClO₄-SiO₂ / water; acetonitrile / 0.33 h / 20 °C

With N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; tetrabutylammomium bromide; sodium hydroxide; In tetrahydrofuran; dichloromethane; water; acetonitrile;

DOI:10.1080/07328300903477804

Reference yield:

ethyl 2,3,4-tri-O-acetyl-1-thio-α-L-rhamnopyranoside (125520-01-6) → methyl (2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-2-O-benzyl-α-D-glucopyranoside (1220097-83-5)

Guidance literature:

Multi-step reaction with 3 steps

1: N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate / dichloromethane / 1 h / -40 °C / Inert atmosphere; Molecular sieve

2: tetrabutylammomium bromide; sodium hydroxide / tetrahydrofuran / 6 h / 20 °C

3: HClO₄-SiO₂ / water; acetonitrile / 0.33 h / 20 °C

With N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; tetrabutylammomium bromide; sodium hydroxide; In tetrahydrofuran; dichloromethane; water; acetonitrile;

DOI:10.1080/07328300903477804

upstream raw materials:

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

ethyl 2,3,4-tri-O-acetyl-1-thio-α-L-rhamnopyranoside

methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside

Downstream raw materials:

methyl (2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1->3)-[(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1->6)]-2-O-benzyl-α-D-glucopyranoside