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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66683Generated: October 27, 2026

Chloride → Ethyl alpha-acetyl-4-(4-fluorobenzoyl)-1-piperidinepentanoate

https://huagongshe.com/reaction/66683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium hydrideHCID 24758—
Reactant[1-(3-Chloropropyl)piperidin-4-yl](4-fluorophenyl)methanoneHCID 12404419—
SolventTolueneHCID 1140—
ProductEthyl alpha-acetyl-4-(4-fluorobenzoyl)-1-piperidinepentanoateHCID 20530727—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a stirred mixture of 4 parts of a sodium hydride dispersion 60% in 180 parts of methylbenzene are added dropwise 12 parts of ethyl 3-oxobutanoate at room temperature. Then there is added 1 part of N,N,N-tridecylmethanammonium chloride and the whole is warmed to 40° C. At this temperature, a solution of 25 parts of [1-(3-chloropropyl)-4-piperidinyl](4-fluorophenyl)methanone in 45 parts of methylbenzene is added slowly. The whole is heated to reflux and stirring is continued overnight at reflux temperature. The reaction mixture is cooled to room temperature and filtered over Hyflo. The filtrate is evaporated, yielding 24 parts of ethyl α-acetyl-4-(4-fluorobenzoyl)-1-piperidinepentanoate as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04342870
Source datasetuspto-grants-1982_08
ORD IDord-7ef74cc1425143db850e7a32adec9fe2
Source noteuspto-grants-1982_08