1-Bromo-2,3,4-trimethoxy-5-(2,3,4,6-tetra-O-methoxycarbonyl-β-D-glucopyranosyl)benzene

Base Information

Chemical Name:1-Bromo-2,3,4-trimethoxy-5-(2,3,4,6-tetra-O-methoxycarbonyl-β-D-glucopyranosyl)benzene
CAS No.:132817-40-4
Molecular Formula:C₂₃H₂₉BrO₁₆
Molecular Weight:641.378
Hs Code.:

Synonyms:1-Bromo-2,3,4-trimethoxy-5-(2,3,4,6-tetra-O-methoxycarbonyl-β-D-glucopyranosyl)benzene

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Chemical Property of 1-Bromo-2,3,4-trimethoxy-5-(2,3,4,6-tetra-O-methoxycarbonyl-β-D-glucopyranosyl)benzene

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Technology Process of 1-Bromo-2,3,4-trimethoxy-5-(2,3,4,6-tetra-O-methoxycarbonyl-β-D-glucopyranosyl)benzene

There total 5 articles about 1-Bromo-2,3,4-trimethoxy-5-(2,3,4,6-tetra-O-methoxycarbonyl-β-D-glucopyranosyl)benzene 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: 88.0%

: 132817-39-1
1,2,3-Trimethoxy-4-(2,3,4,6-tetra-O-methoxycarbonyl-β-D-glucopyranosyl)benzene

: 132817-40-4
1-Bromo-2,3,4-trimethoxy-5-(2,3,4,6-tetra-O-methoxycarbonyl-β-D-glucopyranosyl)benzene

Guidance literature:: With bromine; In chloroform; for 0.25h; Ambient temperature;
DOI:10.1016/0008-6215(91)80148-G

Reference yield:

: 634-36-6
1,2,3-trimethoxybenzene

: 132817-40-4
1-Bromo-2,3,4-trimethoxy-5-(2,3,4,6-tetra-O-methoxycarbonyl-β-D-glucopyranosyl)benzene

Guidance literature:: Multi-step reaction with 4 steps

1: boron trifluoride etherate / CH₂Cl₂ / 0.5 h / Ambient temperature

2: 98 percent / hydrogen / 10 percent Pd-C / methanol; acetic acid / 10 h / Ambient temperature

3: 90 percent / pyridine, 4-dimethylaminopyridine / CH₂Cl₂ / 1.5 h / -10 °C

4: 88 percent / bromine / CHCl₃ / 0.25 h / Ambient temperature

With pyridine; dmap; boron trifluoride diethyl etherate; hydrogen; bromine; palladium on activated charcoal; In methanol; dichloromethane; chloroform; acetic acid;
DOI:10.1016/0008-6215(91)80148-G

Reference yield:

: 132817-37-9
1,2,3-Trimethoxy-4-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)benzene

: 132817-40-4
1-Bromo-2,3,4-trimethoxy-5-(2,3,4,6-tetra-O-methoxycarbonyl-β-D-glucopyranosyl)benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / hydrogen / 10 percent Pd-C / methanol; acetic acid / 10 h / Ambient temperature

2: 90 percent / pyridine, 4-dimethylaminopyridine / CH₂Cl₂ / 1.5 h / -10 °C

3: 88 percent / bromine / CHCl₃ / 0.25 h / Ambient temperature

With pyridine; dmap; hydrogen; bromine; palladium on activated charcoal; In methanol; dichloromethane; chloroform; acetic acid;
DOI:10.1016/0008-6215(91)80148-G