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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429058Generated: November 1, 2026

Hydrochloric Acid → (+/-)-1-(1-Amino-3-butyl)-4-(4-fluorophenyl)piperidine

https://huagongshe.com/reaction/429058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant3-[4-(4-Fluorophenyl)piperidin-1-yl]butanenitrileHCID 91182868—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-1-(1-Amino-3-butyl)-4-(4-fluorophenyl)piperidineHCID 91338801—

Reaction Steps

A solution of (+/−)-1-(1-cyano-2-propyl)-4-(4-fluorophenyl)piperidine (457 mg, 1.85 mmol) in tetrahydrofuran (5 mL) was added dropwise to 1 M borane/tetrahydrofuran (5 mL) under an inert argon atmosphere. The reaction mixture was refluxed for two hours and then cooled to ambient temperature. 6 N HCl (4 mL) was added to the reaction, stirred for 0.5 hour and then the tetrahydrofuran boiled off. The resultant aqueous solution was cooled in an ice bath and made basic by addition solid sodium hydroxide pellets. The product was extracted into methylene chloride, the extract dried (anhydrous sodium sulfate), filtered, and the solvent removed to give the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316437B1
Source datasetuspto-grants-2001_11
ORD IDord-e59753223df547fe98a587abbccc430b
Source noteuspto-grants-2001_11