2,4-di-O-(tert-butyldiphenyl)silyl-6-O-(ethoxycarbonyl)-1-C-phenyl-β-D-glucopyranoside

Base Information

• Chemical Name: 2,4-di-O-(tert-butyldiphenyl)silyl-6-O-(ethoxycarbonyl)-1-C-phenyl-β-D-glucopyranoside
• CAS No.: 1432591-97-3
• Molecular Formula: C₄₇H₅₆O₇Si₂
• Molecular Weight: 789.128
• Mol file: 1432591-97-3.mol

Synonyms:2,4-di-O-(tert-butyldiphenyl)silyl-6-O-(ethoxycarbonyl)-1-C-phenyl-β-D-glucopyranoside

Chemical Property of 2,4-di-O-(tert-butyldiphenyl)silyl-6-O-(ethoxycarbonyl)-1-C-phenyl-β-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2,4-di-O-(tert-butyldiphenyl)silyl-6-O-(ethoxycarbonyl)-1-C-phenyl-β-D-glucopyranoside

There total 5 articles about 2,4-di-O-(tert-butyldiphenyl)silyl-6-O-(ethoxycarbonyl)-1-C-phenyl-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: 96.0%

2,4-di-O-tert-butyldiphenylsilyl-1-C-phenyl-β-D-glucopyranoside (1432591-76-8) + chloroformic acid ethyl ester (541-41-3) → 2,4-di-O-(tert-butyldiphenyl)silyl-6-O-(ethoxycarbonyl)-1-C-phenyl-β-D-glucopyranoside (1432591-97-3)

Guidance literature:

With dmap; triethylamine; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

1,6-anhydro-2,4-di-O-tert-butyldiphenylsilyl-β-D-glucopyranose (1432591-75-7) → 2,4-di-O-(tert-butyldiphenyl)silyl-6-O-(ethoxycarbonyl)-1-C-phenyl-β-D-glucopyranoside (1432591-97-3)

Guidance literature:

Multi-step reaction with 2 steps

1.1: aluminum (III) chloride / tetrahydrofuran; dibutyl ether / 1 h / 0 - 20 °C

1.2: 60 °C / Reflux

2.1: triethylamine; dmap / dichloromethane / 2 h / 20 °C

With dmap; aluminum (III) chloride; triethylamine; In tetrahydrofuran; dichloromethane; dibutyl ether;

Reference yield:

tert-butylchlorodiphenylsilane (58479-61-1) → 2,4-di-O-(tert-butyldiphenyl)silyl-6-O-(ethoxycarbonyl)-1-C-phenyl-β-D-glucopyranoside (1432591-97-3)

Guidance literature:

Multi-step reaction with 3 steps

1.1: 1H-imidazole / tetrahydrofuran / 0 °C

2.1: aluminum (III) chloride / tetrahydrofuran; dibutyl ether / 1 h / 0 - 20 °C

2.2: 60 °C / Reflux

3.1: triethylamine; dmap / dichloromethane / 2 h / 20 °C

With 1H-imidazole; dmap; aluminum (III) chloride; triethylamine; In tetrahydrofuran; dichloromethane; dibutyl ether;

upstream raw materials:

1,6-anhydro-2,4-di-O-tert-butyldiphenylsilyl-β-D-glucopyranose

levoglucosan

tert-butylchlorodiphenylsilane

2,4-di-O-tert-butyldiphenylsilyl-1-C-phenyl-β-D-glucopyranoside

Downstream raw materials:

6-O-(ethoxycarbonyl)-1-C-phenyl-β-D-glucopyranoside (Va)