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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729389Generated: October 26, 2026

Triethylamine → 3-Chloro-2-cyclopropylamino-4,5-difluorobenzoic acid

https://huagongshe.com/reaction/729389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclopropylamineHCID 69828—
ReactantPotassium AcetateHCID 517044—
Reactant2-Bromo-3-chloro-4,5-difluorobenzoic acidHCID 21979471—
SolventIsopropanolHCID 3776—
Product3-Chloro-2-cyclopropylamino-4,5-difluorobenzoic acidHCID 2197893363.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a sealed tube a mixture of 2-bromo-3-chloro-4,5-difluorobenzoic acid (Example 20, 7.96 g, 29.3 mmol), cyclopropyl amine (4.20 mL, 58.7 mmol), potassium acetate (5.77 g, 58.6 mmol), cupric acetate monohydrate (0.50 g, 2.5 mmol), and triethylamine (4.9 mL, 35.19 mmol) in isopropyl alcohol is stirred at 80° C. After 16 hours, the reaction mixture is concentrated under vacuum, and the resulting residue is dissolved in ethyl acetate. The organic layer is washed with 1.0 M hydrochloric acid, water, and brine. The organic layer is dried over MgSO4 and filtered. The filtrate is concentrated under vacuum and purified via flash column chromatography (5% isopropyl alcohol/1% formic acid/94% dichloromethane) to afford the title compound (4.62 g). MS CI: m/z 248 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582627B2
Source datasetuspto-grants-2009_09
ORD IDord-adbdcf04dc094a1aa1bc29a11bda2386
Source noteuspto-grants-2009_09