allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-di-O-benzoyl-α-D-mannopyranoside

Base Information

Chemical Name:allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-di-O-benzoyl-α-D-mannopyranoside
CAS No.:612064-52-5
Molecular Formula:C₅₁H₄₆O₁₆
Molecular Weight:914.917
Hs Code.:

Synonyms:allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-di-O-benzoyl-α-D-mannopyranoside

Suppliers and Price of allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-di-O-benzoyl-α-D-mannopyranoside

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-di-O-benzoyl-α-D-mannopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-di-O-benzoyl-α-D-mannopyranoside

There total 3 articles about allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-di-O-benzoyl-α-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: 86.8%

: 98-88-4
benzoyl chloride

: 612064-51-4
allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-O-benzylidene-α-D-mannopyranoside

: 612064-52-5
allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-di-O-benzoyl-α-D-mannopyranoside

Guidance literature:: allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-O-benzylidene-α-D-mannopyranoside; In water; toluene; trifluoroacetic acid;

benzoyl chloride; In pyridine; at 20 ℃; for 12h;
DOI:10.1016/S0008-6215(03)00264-7

Reference yield:

: 81600-93-3
allyl 4,6-di-O-benzylidene-α-D-mannopyranoside

: 612064-52-5
allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-di-O-benzoyl-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1.1: 90.6 percent / pyridine / CH₂Cl₂ / 2 h / 0 - 20 °C

2.1: 85.1 percent / TMSOTf / CH₂Cl₂ / 2 h / -10 °C

3.1: trifluoroacetic acid; H₂O; toluene

3.2: 86.8 percent / pyridine / 12 h / 20 °C

With pyridine; trimethylsilyl trifluoromethanesulfonate; In dichloromethane; water; toluene; trifluoroacetic acid;
DOI:10.1016/S0008-6215(03)00264-7

Reference yield:

: 612056-98-1
allyl-3-O-acetyl-4,6-O-benzylidene-2-hydroxy-α-D-mannopyranoside

: 612064-52-5
allyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->2)-3-O-acetyl-4,6-di-O-benzoyl-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1.1: 85.1 percent / TMSOTf / CH₂Cl₂ / 2 h / -10 °C

2.1: trifluoroacetic acid; H₂O; toluene

2.2: 86.8 percent / pyridine / 12 h / 20 °C

With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; water; toluene; trifluoroacetic acid;
DOI:10.1016/S0008-6215(03)00264-7