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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426131Generated: November 2, 2026

Triethylamine → 3-Chloro-4-fluoro-benzoic acid 5-(3-chloro-4-fluoro-benzoylamino)-2-methyl-phenyl ester

https://huagongshe.com/reaction/2426131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Amino-2-methylphenolHCID 17818—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Chloro-4-fluorobenzoyl ChlorideHCID 2736548—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-4-fluoro-benzoic acid 5-(3-chloro-4-fluoro-benzoylamino)-2-methyl-phenyl esterHCID 67212789—

Reaction Steps

A solution of 3-chloro-4-fluorobenzoyl chloride (21.23 g, 110 mmol, Avocado) in tetrahydrofuran (50 mL) was added to a solution of 5-amino-o-cresol (6.16 g, 50 mmol, Aldrich) and triethylamine (17.5 mL, 125 mmol, Aldrich) and tetrahydrofuran (50 mL) dropwise with magnetic stirring and cooling in an ice-water bath. When the addition was complete, the mixture was allowed to warm to room temperature and stirred for 16 hours. The mixture was then diluted with water (125 mL) and saturated aqueous sodium bicarbonate solution (125 mL). After stirring for another 30 minutes, the precipitate was collected to give crude 3-chloro-4-fluoro-benzoic acid 5-(3-chloro-4-fluoro-benzoylamino)-2-methyl-phenyl ester as an off-white powder. (Yield 21.83 g, 101%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968554B2
Source datasetuspto-grants-2011_06
ORD IDord-ec286319f10f404d91183fb1810a03ff
Source noteuspto-grants-2011_06