HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929013Generated: October 30, 2026
Methanol → 5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid methyl ester
https://huagongshe.com/reaction/929013
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid | HCID 21866991 | — |
| Product | 5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid methyl ester | HCID 86596771 | 85.8% |
Reaction Steps
To a solution of 5-bromo-3,4-difluoro-2-((2-chlorophenyl)amino)benzoic acid (25.63 g, 70.69 mmol) in MeOH (300 mL) was added thionyl chloride (20 mL). The resulting solution was stirred at 85° C. overnight. Most MeOH was removed in vacuo. The residue was neutralized with saturated sodium bicarbonate (aq.) and extracted with ethyl acetate (100 mL×3). The combined organic layer was washed with water (100 mL) and brine (100 mL) sequentially, dried over Na2SO4, filtered and concentrated. After purification by column chromatography on silica gel (petroleum ether/ethyl acetate, 50:1, v/v), the corresponding product was obtained as a white solid (22.84 g, 85.8% yield). 1H NMR (400 MHz, CDCl3): δ 9.15 (s, 1H), 8.06 (m, 1H), 7.41 (m, 1H), 7.24 (m, 1H), 7.00 (m, 1H), 6.91 (m, 1H), 3.95 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290468B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-3098c12b619f42f6b80077c7b622b190 |
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| Source note | uspto-grants-2016_03 |
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