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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647355Generated: October 27, 2026

Tetrahydrofuran → 4-(2-Fluorobenzoyl)-1-methylpiperidine

https://huagongshe.com/reaction/647355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-FluorobenzonitrileHCID 67855—
Reactant4-chloro-N-methylpiperidineHCID 79342—
ReactantMagnesiumHCID 5462224—
CatalystEthyl BromideHCID 6332—
Product4-(2-Fluorobenzoyl)-1-methylpiperidineHCID 1318031791%

Reaction Steps

To a suspension of 7.6 g of magnesium turnings in 25 ml of tetrahydrofuran was added a few drops of ethyl bromide, with stirring under nitrogen. After the reaction began, approximately 50.0 g of N-methyl-4-chloropiperidine in 125 ml of tetrahydrofuran was added dropwise at a rate such as to maintain moderate reflux. The reaction mixture was heated under reflux an additional hr, and 37.2 g of 2-fluorobenzonitrile in 50 ml of tetrahydrofuran was added dropwise. After completion of the addition, the reaction mixture was refluxed for two hrs, and stirred overnight at room temperature. The reaction mixture was poured into a solution of 85 g of ammonium chloride in 1200 ml of ice water and heated on a steam bath for 3 hrs. The mixture was cooled, extracted with benzene (3×250 ml), dried over anhydrous sodium sulfate, and the excess solvent was removed under reduced pressure to give 62.72 g (91%) of 4-(2-fluorobenzoyl)-1-methyl piperidine as an oil. A small amount of 4-(2-fluorobenzoyl)-1-methyl piperidine (1.0 g) was removed, dissolved in ether and a solution of ethereal hydrochloric acid was added. The precipitate was collected, dried and recrystallized from ethanol-ether (2×) to give 0.5 g of 4-(2-fluorobenzoyl)-1-methyl piperidine hydrochloride, mp, 167°-169°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04408054
Source datasetuspto-grants-1983_10
ORD IDord-1c61c4a072be4114943ad2371e188be2
Source noteuspto-grants-1983_10