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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578389Generated: October 26, 2026

4-(4-Chlorophenyl)-alpha-(4-fluorophenyl)-4-hydroxy-1-piperidinebutanol → Haloperidol

https://huagongshe.com/reaction/1578389

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chlorophenyl)-alpha-(4-fluorophenyl)-4-hydroxy-1-piperidinebutanolHCID 119265—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
ProductHaloperidolHCID 3559—

Reaction Steps

To a solution of 4.0 g of 1-(p-fluorophenyl)-4-[4-(p-chlorophenyl)-4-hydroxypiperidino]-1-butanol in 100 ml of chloroform was added 10 g of manganese dioxide (fine powder). And then the mixture was stirred at room temperature for 7 hours. The reaction product was filtered and the filtrate was concentrated to dryness under reduced pressure. The residue was recrystallized from aqueous acetone to obtain γ-[4-(p-chlorophenyl)-4-hydroxypiperidino]-p-fluorobutyrophenone, melting at 150° - 151°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03936468
Source datasetuspto-grants-1976_02
ORD IDord-c6f6cc5341bd4c88a181803460cd05ba
Source noteuspto-grants-1976_02