2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside

Base Information

• Chemical Name: 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside
• CAS No.: 299424-47-8
• Molecular Formula: C₃₉H₅₈O₇Si₂
• Molecular Weight: 695.056
• Mol file: 299424-47-8.mol

Synonyms:2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside

Chemical Property of 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside

There total 5 articles about 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside 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:

benzyl bromide (100-39-0) + 2-(trimethylsilyl)ethyl 6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside → 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside (299424-47-8)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 4h;

DOI:10.1248/cpb.48.1160

Reference yield:

2-(trimethylsilyl)ethyl β-D-galactopyranoside (117252-95-6) → 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside (299424-47-8)

Guidance literature:

Multi-step reaction with 3 steps

1.1: dibutyltin oxide / methanol / 2 h / Heating

1.2: 66.9 percent / CsF / dimethylformamide / 5 h

2.1: imidazole / dimethylformamide / 3 h / 20 °C

3.1: 605 mg / NaH / dimethylformamide / 4 h / 0 °C

With 1H-imidazole; sodium hydride; di(n-butyl)tin oxide; In methanol; N,N-dimethyl-formamide;

DOI:10.1248/cpb.48.1160

Reference yield:

tert-butyldimethylsilyl chloride (18162-48-6) → 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-p-methoxybenzyl-β-D-galactopyranoside (299424-47-8)

Guidance literature:

Multi-step reaction with 2 steps

1: imidazole / dimethylformamide / 3 h / 20 °C

2: 605 mg / NaH / dimethylformamide / 4 h / 0 °C

With 1H-imidazole; sodium hydride; In N,N-dimethyl-formamide;

DOI:10.1248/cpb.48.1160

upstream raw materials:

benzyl bromide

2-(trimethylsilyl)ethyl β-D-galactopyranoside

tert-butyldimethylsilyl chloride

p-methoxybenzyl chloride

Downstream raw materials:

2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-3-O-p-methoxybenzyl-β-D-galactopyranoside

2-(trimethylsilyl)ethyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->6)-2,4-di-O-benzyl-3-O-p-methoxybenzyl-β-D-galactopyranoside

2-(trimethylsilyl)ethyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranosyl-(1->6)-2,4-di-O-benzyl-β-D-galactopyranoside