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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440794Generated: November 2, 2026

2-Chloro-4'-fluoroacetophenone → HCID 15816464, compound

https://huagongshe.com/reaction/1440794

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4'-fluoroacetophenoneHCID 120248—
ReactantSodium BicarbonateHCID 516892—
ReactantN-[4-(Piperidine-4-carbonyl)phenyl]acetamideHCID 15680074—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 15816464HCID 15816464—

Reaction Steps

To a solution of 3.0 g (12.2 mmol) of N-[4-(4-piperidinyl-carbonyl)phenyl]-acetamide in 10 ml of water and 100 ml of tetrahydrofuran was added 2.3 g (13.4 mmol) of 2-chloro-4'-fluoro-acetophenone followed by 2.0 g (24.4 mmol) of sodium bicarbonate. This mixture was heated to reflux for 1.5 hours. The reaction mixture was poured into 500 ml of brine and extracted with chloroform. The organic layer was dried with magnesium sulfate, filtered and concentrated to yield a solid which was recrystallized from 2-butanone/cyclohexane. 1-(4-Fluorophenyl)-2-[4-[(4acetamidophenyl)carbonyl]-1-piperidinyl]-ethanone was obtained as an off-white solid having amp of 168°-170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500433
Source datasetuspto-grants-1996_03
ORD IDord-c17bb95d9f644febb3070c37881dd837
Source noteuspto-grants-1996_03