3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside

Base Information

• Chemical Name: 3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside
• CAS No.: 309261-83-4
• Molecular Formula: C₆₁H₅₀O₁₈
• Molecular Weight: 1071.06
• Mol file: 309261-83-4.mol

Synonyms:3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside

Chemical Property of 3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside

Chemical Property:

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside

There total 3 articles about 3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-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: 98.0%

1-O-tert-butyldiphenylsilyl-3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside (309261-82-3) → 3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside (309261-83-4)

Guidance literature:

With tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran; Inert atmosphere; Reflux;

DOI:10.1021/ol401044h

Reference yield:

benzoyl chloride (98-88-4) → 3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside (309261-83-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 100 percent / DMAP / pyridine / 25 °C

2: 86 percent / Bu₄NF / tetrahydrofuran / 4 h

With dmap; tetrabutyl ammonium fluoride; In tetrahydrofuran; pyridine; 1: bezoylation / 2: desilylation;

DOI:10.1016/S0008-6215(00)00119-1

Reference yield:

1-O-tert-butyldiphenylsilyl-3,4-di-O-benzoyl-β-D-fructofuranosyl-2,3,4-tri-O-benzoyl-α-D-glucopyranoside (1055037-08-5) → 3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside (309261-83-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 100 percent / DMAP / pyridine / 25 °C

2: 86 percent / Bu₄NF / tetrahydrofuran / 4 h

With dmap; tetrabutyl ammonium fluoride; In tetrahydrofuran; pyridine; 1: bezoylation / 2: desilylation;

DOI:10.1016/S0008-6215(00)00119-1

upstream raw materials:

1-O-tert-butyldiphenylsilyl-3,4,6-tri-O-benzoyl-β-D-fructofuranosyl-2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside

benzoyl chloride

1-O-tert-butyldiphenylsilyl-3,4-di-O-benzoyl-β-D-fructofuranosyl-2,3,4-tri-O-benzoyl-α-D-glucopyranoside

Downstream raw materials:

1'-O-trifluoromethanesulfonyl-2,3,4,6,3',4',6'-,hepta-O-benzoylsucrose