1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranose

Base Information

Chemical Name:1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranose
CAS No.:131157-69-2
Molecular Formula:C₆₁H₅₀O₁₈
Molecular Weight:1071.06
Hs Code.:

Synonyms:1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranose

Suppliers and Price of 1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranose

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

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Chemical Property of 1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranose

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranose

There total 1 articles about 1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranose 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: 76.0%

: 58166-26-0
leucrose (O-α-D-glucopyranosyl-(1-5)-D-fructopyranose)

: 98-88-4
benzoyl chloride

: 131157-69-2
1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranose

Guidance literature:: With pyridine; Ambient temperature;
DOI:10.1016/0008-6215(90)80151-R

Reference yield: 86.0%

: 131157-69-2
1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranose

: 131157-70-5
1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranosyl bromide

Guidance literature:: With hydrogen bromide; In acetic acid; for 5h; Ambient temperature;
DOI:10.1016/0008-6215(90)80151-R

Reference yield:

: 131157-69-2
1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-β-D-fructopyranose

: 131157-72-7
1,5-anhydro-3,4-di-O-benzoyl-6-deoxy-2-O-(2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl)-D-mannitol

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / HBr / acetic acid / 5 h / Ambient temperature

2: 65 percent / sodium acetate, zinc dust, copper sulfate pentahydrate / H₂O; acetic acid / 3 h / -10 °C

3: 53 percent / H₂ / 33percent Pd-C / ethyl acetate / 16 h / Ambient temperature

With hydrogen bromide; hydrogen; sodium acetate; copper(II) sulfate; zinc; palladium on activated charcoal; In water; acetic acid; ethyl acetate;
DOI:10.1016/0008-6215(90)80151-R