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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26175Generated: October 30, 2026

Hydrochloric Acid → gamma-(4-Benzyl-4-hydroxypiperidino)-2-chlorobutyrophenone hydrochloride

https://huagongshe.com/reaction/26175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantgamma-(4-Benzyl-4-hydroxypiperidino)-2-aminobutyrophenoneHCID 21324676—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Productgamma-(4-Benzyl-4-hydroxypiperidino)-2-chlorobutyrophenone hydrochlorideHCID 86736453—

Reaction Steps

To a cooled solution of 3.6 g of γ-(4-benzyl-4-hydroxypiperidino)-2-aminobutyrophenone in 35 ml of 2N hydrochloric acid was added dropwise a solution of 0.74 g of sodium nitrite in 5 ml of water with stirring below 0° C. The resulting diazonium salt solution was added all at once to a cold suspension of 1.5 g of cuprous chloride in 5 ml of concentrated hydrochloric acid with vigorous stirring. The mixture was stirred for 30 minutes under cooling with ice, and stirring was continued for 2 hours at room temperature and then for 1 hour at 55°-60° C. After cooling, the reaction mixture was made alkaline, and extracted with chloroform. The extract was washed with water, dried and concentrated to a residue. The residue was treated with methanolic hydrogen chloride and recrystallization of the resulting solid matter from isopropanol gave γ-(4-benzyl-4-hydroxypiperidino)-2-chlorobutyrophenone hydrochloride.8c

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04148796
Source datasetuspto-grants-1979_04
ORD IDord-72b3ad87da5a47c7958a2a715a962bb0
Source noteuspto-grants-1979_04