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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929036Generated: October 30, 2026

Methanol → Methyl 5-bromo-2-(2-fluorophenylamino)-3,4-difluorobenzoate

https://huagongshe.com/reaction/929036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Bromo-3,4-difluoro-2-((2-fluorophenyl)amino)benzoic acidHCID 59519388—
ProductMethyl 5-bromo-2-(2-fluorophenylamino)-3,4-difluorobenzoateHCID 5951939188.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 5-bromo-3,4-difluoro-2-((2-fluorophenyl)amino)benzoic acid (24.24 g, 70.04 mmol) in MeOH (300 mL) was added thionyl chloride (20 mL). After stirring 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 (22.33 g, 88.5% yield). 1H NMR (400 MHz, CDCl3): δ 9.06 (s, 1H), 8.01 (dd, J=7.1, 2.3 Hz, 1H), 7.04 (m, 4H), 3.92 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290468B2
Source datasetuspto-grants-2016_03
ORD IDord-4af0b3a3ee42460e83a777835e1c98e6
Source noteuspto-grants-2016_03