5,4'-di-O-hexanoylapigenin-7-yl-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside

Base Information

Chemical Name:5,4'-di-O-hexanoylapigenin-7-yl-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside
CAS No.:1145669-48-2
Molecular Formula:C₆₁H₅₆O₁₆
Molecular Weight:1045.11
Hs Code.:

Synonyms:5,4'-di-O-hexanoylapigenin-7-yl-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside

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Chemical Property of 5,4'-di-O-hexanoylapigenin-7-yl-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside

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Technology Process of 5,4'-di-O-hexanoylapigenin-7-yl-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside

There total 3 articles about 5,4'-di-O-hexanoylapigenin-7-yl-2,3,4,6-tetra-O-benzoyl-β-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: 79.0%

: 14218-11-2
2,3,4,6-tetra-O-benzoylglucosyl bromide

: 1145669-47-1
5,4'-di-O-hexanoyl-apigenin

: 1145669-48-2
5,4'-di-O-hexanoylapigenin-7-yl-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside

Guidance literature:: With tetrabutylammomium bromide; potassium carbonate; In chloroform; water; at 40 ℃; for 24h;
DOI:10.1016/j.tetlet.2018.11.015

Reference yield:

: 520-36-5
5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

: 1145669-48-2
5,4'-di-O-hexanoylapigenin-7-yl-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine; dmap / N,N-dimethyl-formamide / 4.5 h / 20 °C / Cooling with ice

2: potassium carbonate / methanol; dichloromethane / 20 °C

3: potassium carbonate; tetrabutylammomium bromide / chloroform; water / 24 h / 40 °C

With dmap; tetrabutylammomium bromide; potassium carbonate; triethylamine; In methanol; dichloromethane; chloroform; water; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2018.11.015

Reference yield:

: 142-61-0
Hexanoyl chloride

: 1145669-48-2
5,4'-di-O-hexanoylapigenin-7-yl-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine; dmap / N,N-dimethyl-formamide / 4.5 h / 20 °C / Cooling with ice

2: potassium carbonate / methanol; dichloromethane / 20 °C

3: potassium carbonate; tetrabutylammomium bromide / chloroform; water / 24 h / 40 °C

With dmap; tetrabutylammomium bromide; potassium carbonate; triethylamine; In methanol; dichloromethane; chloroform; water; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2018.11.015