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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acidHCID 21866991—
Product5-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid methyl esterHCID 8659677185.8%

Reaction Conditions

Temperature85 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290468B2
Source datasetuspto-grants-2016_03
ORD IDord-3098c12b619f42f6b80077c7b622b190
Source noteuspto-grants-2016_03