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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645225Generated: November 1, 2026

Tetrahydrofuran → HCID 3772327, compound

https://huagongshe.com/reaction/1645225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl trifluoroacetateHCID 9794—
ReactantSodium ethoxideHCID 2723922—
Reactant1-(3-Chloro-5-trifluoromethyl-pyridin-2-yl)-ethanoneHCID 21712136—
SolventWaterHCID 962—
ProductHCID 3772327HCID 377232798%

Reaction Steps

608 mg of a sodium ethoxide 21% ethanol solution was added at 0° C. to a tetrahydrofuran (dehydrated) 9 mL solution of 1 g of 2-acetyl-3-chloro-5-(trifluoromethyl)pyridine and 635 mg of ethyl 2,2,2-trifluoroacetate, followed by stirring at room temperature for 13 hours. After completion of the reaction, water was added to the reaction liquid, followed by extraction with ethyl acetate, the organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 1.4 g of 1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)-4,4,4-trifluorobutan-1,3-dione (after-mentioned intermediate No. IX-25).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124760B2
Source datasetuspto-grants-2012_02
ORD IDord-79ad4b602d2a42eeb48367943b2540fb
Source noteuspto-grants-2012_02