2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1→6)]-2-O-acetyl-β-D-glucopyranoside

Base Information

• Chemical Name: 2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1→6)]-2-O-acetyl-β-D-glucopyranoside
• CAS No.: 1436383-93-5
• Molecular Formula: C₄₂H₅₆O₂₃
• Molecular Weight: 928.893
• Mol file: 1436383-93-5.mol

Synonyms:2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1→6)]-2-O-acetyl-β-D-glucopyranoside

Chemical Property of 2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1→6)]-2-O-acetyl-β-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1→6)]-2-O-acetyl-β-D-glucopyranoside

There total 3 articles about 2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1→6)]-2-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: 71.0%

2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-2-O-acetyl-β-D-glucopyranoside (1436383-92-4) + O-(2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl)-trifluoracetimidat (92052-33-0) → 2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1→6)]-2-O-acetyl-β-D-glucopyranoside (1436383-93-5)

Guidance literature:

With nitrosonium tetrafluoroborate; In dichloromethane; at -35 ℃; for 0.5h; Inert atmosphere;

DOI:10.3762/bjoc.9.80

Reference yield:

C33H40O13 → 2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1→6)]-2-O-acetyl-β-D-glucopyranoside (1436383-93-5)

Guidance literature:

Multi-step reaction with 3 steps

1: dichloromethane / 1 h / 20 °C / Inert atmosphere

2: palladium 10% on activated carbon; triethylsilane / methanol; dichloromethane / 0.5 h / 20 °C

3: nitrosonium tetrafluoroborate / dichloromethane / 0.5 h / -35 °C / Inert atmosphere

With triethylsilane; palladium 10% on activated carbon; nitrosonium tetrafluoroborate; In methanol; dichloromethane;

DOI:10.3762/bjoc.9.80

Reference yield:

2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-2-O-acetyl-4,6-O-benzylidene-β-D-glucopyranoside (1436383-91-3) → 2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-[2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl-(1→6)]-2-O-acetyl-β-D-glucopyranoside (1436383-93-5)

Guidance literature:

Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; triethylsilane / methanol; dichloromethane / 0.5 h / 20 °C

2: nitrosonium tetrafluoroborate / dichloromethane / 0.5 h / -35 °C / Inert atmosphere

With triethylsilane; palladium 10% on activated carbon; nitrosonium tetrafluoroborate; In methanol; dichloromethane;

DOI:10.3762/bjoc.9.80

upstream raw materials:

2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-2-O-acetyl-β-D-glucopyranoside

O-(2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl)-trifluoracetimidat

2-phenylethyl (2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-(1→3)-2-O-acetyl-4,6-O-benzylidene-β-D-glucopyranoside

Downstream raw materials:

2-phenylethyl (α-L-rhamnopyranosyl)-(1→3)-[β-D-glucopyranosyl-(1→6)]-β-D-glucopyranoside