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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307937Generated: November 1, 2026

Ethyl trifluoroacetate → 4,4,4-Trifluoro-1-(pyridin-2-yl)butane-1,3-dione

https://huagongshe.com/reaction/2307937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
Reactant2-AcetylpyridineHCID 14286—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product4,4,4-Trifluoro-1-(pyridin-2-yl)butane-1,3-dioneHCID 277147881.2%

Reaction Steps

Trifluoro-acetic acid ethyl ester (9.82 mL, 82.5 mmol) was added to a solution of 1-pyridin-2-yl-ethanone (5.00 g, 41.2 mmol) in methanol (40 mL) containing sodium methoxide (61.8 mmol). The reaction mixture was heated at reflux overnight, concentrated under reduced pressure and acidified with aqueous hydrochloric acid (10%). The aqueous solution was extracted with ethyl acetate (10×50 mL). The organic layers were collected, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel to give 4,4,4-trifluoro-1-pyridin-2-yl-butane-1,3-dione (7.26 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833371B2
Source datasetuspto-grants-2004_12
ORD IDord-0952ca7095e04875bd12314b10e9184c
Source noteuspto-grants-2004_12