HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41173Generated: October 26, 2026
Methanol → Methyl 3-acetyl-5-bromo-4-hydroxybenzoate
https://huagongshe.com/reaction/41173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Acetyl-5-bromo-4-hydroxybenzoic acid | HCID 12486469 | — |
| Product | Methyl 3-acetyl-5-bromo-4-hydroxybenzoate | HCID 15818980 | 42.7% |
Reaction Steps
To a stirred suspension of 3-acetyl-5-bromo-4-hydroxybenzoic acid (240 g, 926 mmol) in MeOH (2 L) was added dropwise sulfurous dichloride (68 mL, 926.5 mmol) under nitrogen and the mixture was heated at 80° C. for 3 h. The reaction mixture was cooled to room temperature concentrated, diluted with DCM. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated to afford a crude compound, which was purified on silica, eluting with 70% of DCM in petroleum ether. The solvents were evaporated to dryness to afford methyl 3-acetyl-5-bromo-4-hydroxybenzoate (108 g, 42.7%) as a white powder. Mass Spectrum: m/z [M−H]−=229.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530470B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-097d35d2104149368b95f0854fbb5d30 |
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| Source note | uspto-grants-2013_09 |
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