4-nitrophenyl 6-O-tert-butyldiphenylsilyl-β-D-mannopyranoside

Base Information

• Chemical Name: 4-nitrophenyl 6-O-tert-butyldiphenylsilyl-β-D-mannopyranoside
• CAS No.: 126777-60-4
• Molecular Formula: C₂₈H₃₃NO₈Si
• Molecular Weight: 539.657
• Mol file: 126777-60-4.mol

Synonyms:4-nitrophenyl 6-O-tert-butyldiphenylsilyl-β-D-mannopyranoside

Chemical Property of 4-nitrophenyl 6-O-tert-butyldiphenylsilyl-β-D-mannopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-nitrophenyl 6-O-tert-butyldiphenylsilyl-β-D-mannopyranoside

There total 1 articles about 4-nitrophenyl 6-O-tert-butyldiphenylsilyl-β-D-mannopyranoside 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: 96.5%

4-nitrophenyl-β-D-mannopyranoside (35599-02-1) + tert-butylchlorodiphenylsilane (58479-61-1) → 4-nitrophenyl 6-O-tert-butyldiphenylsilyl-β-D-mannopyranoside (126777-60-4)

Guidance literature:

With 1H-imidazole; In N,N-dimethyl-formamide; at 0 ℃; for 2h;

DOI:10.1016/0008-6215(89)85112-2

Reference yield: 94.0%

4-nitrophenyl 6-O-tert-butyldiphenylsilyl-β-D-mannopyranoside (126777-60-4) + 2,2-dimethoxy-propane (77-76-9) → 4-nitrophenyl 6-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-β-D-mannopyranoside (126777-61-5)

Guidance literature:

With toluene-4-sulfonic acid; In acetone; for 4h; Ambient temperature;

DOI:10.1016/0008-6215(89)85112-2

Reference yield:

4-nitrophenyl 6-O-tert-butyldiphenylsilyl-β-D-mannopyranoside (126777-60-4) → 4-nitrophenyl 2,3-O-isopropylidene-β-D-mannopyranoside (126777-62-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 94 percent / p-toluenesulfonic acid monohydrate / acetone / 4 h / Ambient temperature

2: 98 percent / 1M tetrabutylammonium fluoride / various solvent(s) / 2 h / Ambient temperature

With tetrabutyl ammonium fluoride; toluene-4-sulfonic acid; In acetone;

DOI:10.1016/0008-6215(89)85112-2

upstream raw materials:

4-nitrophenyl-β-D-mannopyranoside

tert-butylchlorodiphenylsilane

Downstream raw materials:

4-nitrophenyl 6-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-β-D-mannopyranoside

4-nitrophenyl 2,3-O-isopropylidene-β-D-mannopyranoside

4-nitrophenyl O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-α-D-mannopyranosyl-(1->6)-2,3-O-isopropylidene-β-D-mannopyranoside

4-nitrophenyl O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-(1->2)-O-(3,4,6-tri-O-acetyl-α-D-mannopyranosyl)(1->6)-2,3-O-isopropylidene-β-D-mannopyranoside