benzyl 1,3,4,6-tetra-O-acetylhex-2-ulofuranoside

Base Information

• Chemical Name: benzyl 1,3,4,6-tetra-O-acetylhex-2-ulofuranoside
• CAS No.: 10225-44-2
• Molecular Formula: C₂₁H₂₆O₁₀
• Molecular Weight: 438.431
• Mol file: 10225-44-2.mol

Synonyms:NSC51256

Chemical Property of benzyl 1,3,4,6-tetra-O-acetylhex-2-ulofuranoside

Chemical Property:

• Vapor Pressure: 1.14E-10mmHg at 25°C
• Boiling Point: 513.8°Cat760mmHg
• Flash Point: 221°C
• Density: 1.27g/cm³

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of benzyl 1,3,4,6-tetra-O-acetylhex-2-ulofuranoside

There total 3 articles about benzyl 1,3,4,6-tetra-O-acetylhex-2-ulofuranoside 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:

methyl α-D-fructofuranoside (13403-14-0,15219-93-9,16975-88-5,51295-55-7,51295-56-8,52443-09-1,60504-77-0,60504-79-2,63526-47-6,69460-17-9,92283-23-3) → benzyl-(tetra-O-acetyl-α-D-fructofuranoside) (10225-44-2)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogen chloride

2: pyridine

With pyridine; hydrogenchloride;

DOI:10.1021/ja01280a012

Reference yield:

benzyl alcohol (100-51-6,185532-71-2) → benzyl-(tetra-O-acetyl-α-D-fructofuranoside) (10225-44-2)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogen chloride

2: pyridine

With pyridine; hydrogenchloride;

DOI:10.1021/ja01280a012

Reference yield:

benzyl α-D-fructofuranoside (76880-54-1) + acetic anhydride (108-24-7) → benzyl-(tetra-O-acetyl-α-D-fructofuranoside) (10225-44-2)

Guidance literature:

With pyridine;

DOI:10.1021/ja01280a012

upstream raw materials:

benzyl α-D-fructofuranoside

acetic anhydride

methyl α-D-fructofuranoside

benzyl alcohol