HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639794Generated: November 3, 2026
Methanol → Methyl 3-amino-6-bromo-2-methylbenzoate
https://huagongshe.com/reaction/1639794
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3-Amino-2-methylbenzoic acid methyl ester | HCID 3801025 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sodium Thiosulfate | HCID 24477 | — |
| Product | Methyl 3-amino-6-bromo-2-methylbenzoate | HCID 59145915 | 55% |
Reaction Steps
To a mixture of methyl 3-amino-2-methylbenzoate (5.00 mL, 34.7 mmol) in acetic acid (100 mL)-methanol (200 mL) was added bromine (5.55 g, 34.7 mmol) under ice-cooling, and the mixture was stirred for 5 min. The reaction solution was diluted with saturated aqueous sodium thiosulfate solution, and the organic solvent was evaporated under reduced pressure. The residual aqueous solution was diluted with saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=5/95→20/80) to give the title compound (4.66 g, yield 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110585B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-91383f919407435f8df3d10266d830e1 |
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| Source note | uspto-grants-2012_02 |
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