HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502770Generated: October 26, 2026
2,3,4-Trimethoxybenzoic acid → 5-Bromo-2,3,4-trimethoxybenzoic acid
https://huagongshe.com/reaction/502770
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3,4-Trimethoxybenzoic acid | HCID 11308 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Bromo-2,3,4-trimethoxybenzoic acid | HCID 59427885 | — |
Reaction Steps
To a solution of 2,3,4-trimethoxybenzoic acid (4.7 g, 22 mmol) and NaOAc (5.5 g, 40 mmol) in 35 ml AcOH was added a solution of bromine (1.5 ml, 29 mmol) in 35 ml AcOH. The reaction became red in color, which quickly faded. The mixture was heated to 80° C. for 1 h, at which point it was cooled to ambient temperature. The material was partitioned between dichloromethane and water. The organic layer was removed and the aqueous layer was extracted once with dichloromethane. The combined organic layers were dried with Na2SO4, filtered, and concentrated to give an oil which solidified on standing. The material was dissolved in diethyl ether and hexanes. Concentration to ½ the volume resulted in precipitation of a white solid. Filtration provided the title compound as a white solid. MS m/z: 293 (M+H+); calc'd for C10H11BrO5: 291.1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776869B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-cdacedadcb22463faf9b0c619e09fb73 |
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| Source note | uspto-grants-2010_08 |
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