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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242001Generated: October 29, 2026

Ethyl 4,4,4-trifluoroacetoacetate → HCID 178516136, compound

https://huagongshe.com/reaction/2242001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4,4,4-trifluoroacetoacetateHCID 67793—
Reactant2-Chloro-5-fluoroanilineHCID 2736509—
SolventWaterHCID 962—
ProductHCID 178516136HCID 17851613651%

Reaction Conditions

Temperature150 °C

Reaction Steps

A solution of ethyl 4,4,4-trifluoroacetoacetate (commercially available, 4 mL, 27.3 mmol, 1.05 eq.) in polyphosphoric acid (22 mL) was heated to 100° C. 2-chloro-5-fluoroaniline (3.78 g, 26.0 mmol, 1 eq.) was added slowly to the stirred hot solution. The resulting reaction mixture was further heated to 150° C. and then stirred at that temperature overnight (approximately 18 hours). The reaction was cooled to room temperature and water was added carefully. The resulting light brown precipitate was collected by vacuum filtration, washed with water and dissolved in ethyl acetate. The ethyl acetate solution was washed with brine, dried over anhydrous MgSO4 and concentrated on a rotary evaporator. The crude product was purified by flash chromatography on silica gel using hexane/ethyl acetate to give 3.54 g (51% yield) of the desired product as an off-white solid; MP=141-142; MS (ES) m/z (relative intensity): 266 (M+H)+ (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671056B2
Source datasetuspto-grants-2010_03
ORD IDord-e3ee1ae27c3f456392c90021689ebb8a
Source noteuspto-grants-2010_03