HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175291Generated: November 1, 2026
Methanol → Methyl 5-amino-2-bromo-4-methylbenzoate
https://huagongshe.com/reaction/1175291
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Amino-2-bromo-4-methylbenzoic acid | HCID 53330275 | — |
| Product | Methyl 5-amino-2-bromo-4-methylbenzoate | HCID 56924477 | 99% |
Reaction Steps
To a cooled solution (5° C.) of 5-amino-2-bromo-4-methylbenzoic acid (100.0 g, 0.434 mmol) in anhydrous methanol (1.6 L) was added dropwise thionyl chloride (112.4 g). The reaction mixture was refluxed and monitored by TLC. After refluxing for 6 h, the reaction was complete. The reaction solution was concentrated under reduced pressure. The residue was diluted with ice water (1.2 L) and neutralized with 5% NaHCO3 to pH 7.5. The aqueous layer was extracted with EtOAc (3×600 mL), and the combined organic layers were washed with brine (2×500 mL), and dried over anhydrous Na2SO4. Concentration under reduced pressure provided the title compound as a pale solid. Yield: 99%. 1H-NMR (DMSO-d6, 300 MHz): δ 7.25 (s, 1H), 7.14 (s, 1H), 3.30 (s, 3H), 2.15 (s, 3H); MS ESI (m/z) 244 [M+1]+, calc. 243.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838498B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-cb5ccf410c4f4f798ac3dd303f1e4275 |
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| Source note | uspto-grants-2010_11 |
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