Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413788Generated: November 2, 2026

Hydrochloric Acid → HCID 23045641, compound

https://huagongshe.com/reaction/2413788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAllyl bromideHCID 7841—
ReactantSodium HydroxideHCID 14798—
Reactant3-(1-Propylpiperidin-3-yl)phenol--hydrogen chloride (1/1)HCID 157471—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
ProductHCID 23045641HCID 23045641—

Reaction Steps

(-)N-n-propyl-3-(3-hydroxyphenyl)piperidine hydrochloride (0.255 g, 1 mmol) and tetrabutylammonium hydrogen sulphate (0.340 g, 1 mmol) were suspended in dichloromethane (2 ml) and allylbromide (0.133 g, 1.1 mmol). 2-M NaOH (2 ml) was added during two minutes and the mixture was stirred at room temperature for half an hour. The layers were separated and the organic layer was dried over Na2SO4. After removal of the solvent by distillation, the residual oil was dissolved in ether (50 ml). A theoretical quantity of tetrabutylammonium iodide was precipitated. The precipitate was filtered off and to the filtrate was added one equivalent HCl-saturated ether. White crystals of the desired compound was obtained. The crystals were filtered, washed on the filters with ether and dried. Yield 190 mg (65%). Mp. 136°-138° C. [α]D20 (C=1.5 MeOH) (-)7.6°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04719219
Source datasetuspto-grants-1988_01
ORD IDord-376e528b4a1b46c183939a1db3829d30
Source noteuspto-grants-1988_01