p-trifluoroacetamidophenyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside

Base Information

• Chemical Name: p-trifluoroacetamidophenyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside
• CAS No.: 118349-74-9
• Molecular Formula: C₃₅H₃₄F₃NO₇
• Molecular Weight: 637.653
• Mol file: 118349-74-9.mol

Synonyms:

Chemical Property of p-trifluoroacetamidophenyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of p-trifluoroacetamidophenyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside

There total 4 articles about p-trifluoroacetamidophenyl 2,3,6-tri-O-benzyl-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:

1-O-(p-nitrophenyl)-4,6-O-benzylidene-β-D-glucopyranoside (118396-60-4) → p-trifluoroacetamidophenyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside (118349-74-9)

Guidance literature:

Multi-step reaction with 3 steps

1: 71 percent / sodium hydride / dimethylformamide

2: 92 percent / hydrogen chloride, sodium cyanoborohydride / tetrahydrofuran; diethyl ether / 0 °C

3: 1.) aluminum amalgam / 1.) tetrahydrofuran-water, 30 min; 2.) pyridine, 0 deg C, 30 min

With hydrogenchloride; aluminium amalgam; sodium hydride; sodium cyanoborohydride; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;

DOI:10.1016/0008-6215(88)84107-7

Reference yield:

p-nitrophenyl 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside (118349-72-7) → p-trifluoroacetamidophenyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside (118349-74-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 92 percent / hydrogen chloride, sodium cyanoborohydride / tetrahydrofuran; diethyl ether / 0 °C

2: 1.) aluminum amalgam / 1.) tetrahydrofuran-water, 30 min; 2.) pyridine, 0 deg C, 30 min

With hydrogenchloride; aluminium amalgam; sodium cyanoborohydride; In tetrahydrofuran; diethyl ether;

DOI:10.1016/0008-6215(88)84107-7

Reference yield:

benzyl bromide (100-39-0) → p-trifluoroacetamidophenyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside (118349-74-9)

Guidance literature:

Multi-step reaction with 3 steps

1: 71 percent / sodium hydride / dimethylformamide

2: 92 percent / hydrogen chloride, sodium cyanoborohydride / tetrahydrofuran; diethyl ether / 0 °C

3: 1.) aluminum amalgam / 1.) tetrahydrofuran-water, 30 min; 2.) pyridine, 0 deg C, 30 min

With hydrogenchloride; aluminium amalgam; sodium hydride; sodium cyanoborohydride; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;

DOI:10.1016/0008-6215(88)84107-7

upstream raw materials:

p-nitrophenyl 2,3,6-tri-O-benzyl-β-D-glucopyranoside

trifluoroacetic anhydride

benzyl bromide

1-O-(p-nitrophenyl)-4,6-O-benzylidene-β-D-glucopyranoside

Downstream raw materials:

p-trifluoroamidophenyl β-D-glycopyranoside 4-(D-ribit-5-yl phosphate)