Benzyl-5-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-fructopyranosid

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Chemical Name:Benzyl-5-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-fructopyranosid
CAS No.:124040-58-0
Molecular Formula:C₄₇H₅₂O₁₁
Molecular Weight:792.923
Hs Code.:

Synonyms:Benzyl-5-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-fructopyranosid

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Chemical Property of Benzyl-5-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-fructopyranosid

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Technology Process of Benzyl-5-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-fructopyranosid

There total 3 articles about Benzyl-5-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-fructopyranosid 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: 84.0%

: 124040-55-7
Benzyl-1,3,4-tri-O-benzoyl-5-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-fructopyranosid

: 124040-58-0
Benzyl-5-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-fructopyranosid

Guidance literature:: With sodium methylate; In methanol; dichloromethane; for 18h; Ambient temperature;
DOI:10.1016/0008-6215(89)84086-8

Reference yield:

: 89025-46-7
2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl fluoride

: 124040-58-0
Benzyl-5-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-fructopyranosid

Guidance literature:: Multi-step reaction with 2 steps

1: BF₃*Et₂O / 21 h / Ambient temperature

2: 84 percent / MeONa / methanol; CH₂Cl₂ / 18 h / Ambient temperature

With sodium methylate; boron trifluoride diethyl etherate; In methanol; dichloromethane;
DOI:10.1016/0008-6215(89)84086-8

Reference yield:

: 124040-50-2
benzyl 1,3,4-tri-O-benzoyl-β-D-fructopyranoside

: 124040-58-0
Benzyl-5-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-β-D-fructopyranosid

Guidance literature:: Multi-step reaction with 2 steps

1: BF₃*Et₂O / 21 h / Ambient temperature

2: 84 percent / MeONa / methanol; CH₂Cl₂ / 18 h / Ambient temperature

With sodium methylate; boron trifluoride diethyl etherate; In methanol; dichloromethane;
DOI:10.1016/0008-6215(89)84086-8