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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730364Generated: November 1, 2026

4-Chlorobenzoyl chloride → HCID 21430572, compound

https://huagongshe.com/reaction/1730364

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
Reactant4-Amino-1-(4-phenyl-4-oxobutyl)piperidine dihydrochlorideHCID 22754837—
ProductHCID 21430572HCID 21430572—

Reaction Steps

4-Amino-1-(4-phenyl-4-oxobutyl)piperidine dihydrochloride (3.19 g.) was acylated with p-chloro-benzoyl chloride (1.75 g.) in the manner of example75. Filtration afforded the title compound as the base (3.277 g.). This wassuspended in boiling ethanol (15 ml). and ethanol/HCl added until acid. On cooling the title compound crystallised out as the hydrochloride, colourless needles (3.41 g.), m.p. 261.1°. Analysis: Found: C, 62.89; H, 6.33; N, 6.64. C22H25CIN2O2.HCl requires C, 62.69; H, 6.22; N, 6.65%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03992389
Source datasetuspto-grants-1976_11
ORD IDord-0e13a9740223465a81a0b7e998479cad
Source noteuspto-grants-1976_11