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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652126Generated: October 29, 2026

Hydrochloric Acid → (2-Fluorophenyl)(1-methylpiperidin-4-yl)methanone--hydrogen chloride (1/1)

https://huagongshe.com/reaction/652126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-FluorobenzonitrileHCID 67855—
Reactant4-chloro-N-methylpiperidineHCID 79342—
ReactantMagnesiumHCID 5462224—
CatalystEthyl BromideHCID 6332—
SolventDiethyl EtherHCID 3283—
Product(2-Fluorophenyl)(1-methylpiperidin-4-yl)methanone--hydrogen chloride (1/1)HCID 1318031842%

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 that moderate reflux was maintained. The reaction was heated under reflux for an additional hour. A solution of 37.2 g of o-fluorobenzonitrile in 30 ml of tetrahydrofuran was added dropwise. After completion of the addition the reaction mixture was heated under reflux 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) and dried over anhydrous sodium sulfate. Removal of the solvent under reduced pressure gave an oil. A 1.0 g-portion of the oil was dissolved in ether and a solution of ethereal hydrogen chloride was added. The precipitate was collected, dried and twice recrystallized from ethanol-ether to give 0.5 g (42%) of product, mp. 167°-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04670447
Source datasetuspto-grants-1987_06
ORD IDord-ee814adf681f4a8193746d8de2ea7d74
Source noteuspto-grants-1987_06