benzyl 3,4-di-O-benzyl-2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside

Base Information

• Chemical Name: benzyl 3,4-di-O-benzyl-2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside
• CAS No.: 73223-28-6
• Molecular Formula: C₃₉H₄₆O₁₂
• Molecular Weight: 706.787
• Mol file: 73223-28-6.mol

Synonyms:benzyl 3,4-di-O-benzyl-2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside

Chemical Property of benzyl 3,4-di-O-benzyl-2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of benzyl 3,4-di-O-benzyl-2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside

There total 3 articles about benzyl 3,4-di-O-benzyl-2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-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: 68.8%

benzyl 3,4-di-O-benzyl-α-L-rhamnopyranoside (62774-10-1) + 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide (5158-64-5) → benzyl 3,4-di-O-benzyl-2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside (73223-28-6)

Guidance literature:

With mercury(II) cyanide; In acetonitrile; for 24h; Ambient temperature;

DOI:10.1016/0008-6215(86)80015-5

Reference yield:

benzyl 2-O-allyl-4-O-benzyl-α-L-rhamnopyranoside (69558-10-7) → benzyl 3,4-di-O-benzyl-2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside (73223-28-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 51 percent / potassium hydroxide / 3 h / 100 °C

2: Hg(CN)2, 4 A molecular sieve / acetonitrile / 48 h / Ambient temperature

With potassium hydroxide; 4 A molecular sieve; mercury(II) cyanide; In acetonitrile;

DOI:10.1016/S0008-6215(00)85921-2

Reference yield:

benzyl chloride (100-44-7) → benzyl 3,4-di-O-benzyl-2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside (73223-28-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 51 percent / potassium hydroxide / 3 h / 100 °C

2: Hg(CN)2, 4 A molecular sieve / acetonitrile / 48 h / Ambient temperature

With potassium hydroxide; 4 A molecular sieve; mercury(II) cyanide; In acetonitrile;

DOI:10.1016/S0008-6215(00)85921-2

upstream raw materials:

benzyl 3,4-di-O-benzyl-α-L-rhamnopyranoside

2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide

benzyl 2-O-allyl-4-O-benzyl-α-L-rhamnopyranoside

benzyl chloride

Downstream raw materials:

benzyl 3,4-di-O-benzyl-2-O-α-L-rhamnopyranosyl-α-L-rhamnopyranoside

benzyl 3,4-di-O-benzyl-2-O-(2,3-O-isopropylidene-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside

benzyl 3,4-di-O-benzyl-2-O-<2,3-O-isopropylidene-4-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside

benzyl 3,4-di-O-benzyl-2-O-<4-O-<2,3-di-O-acetyl-4-O-(2,4-di-O-acetyl-3-O-methyl-β-L-xylopyranosyl)-α-L-rhamnopyrnosyl>-2,3-O-isopropylidene-α-L-rhamnopyranosyl>-α-L-rhamnopyranoside