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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110832Generated: November 2, 2026

Borane;tetrahydrofuran → 4-Aminomethyl-1-(1-naphthylsulfonyl)piperidine

https://huagongshe.com/reaction/2110832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant1-(Naphthylsulfonyl)piperidine-4-carboxamideHCID 23993292—
SolventTetrahydrofuranHCID 8028—
Product4-Aminomethyl-1-(1-naphthylsulfonyl)piperidineHCID 6886203090%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-aminocarbonyl-1-(1-naphthylsulfonyl)piperidine (10.6 g, 33.3 mmol) in tetrahydrofuran (200 mL) stirring under argon at room temperature, was added borane-tetrahydrofuran complex (1.5 M in tetrahydrofuran, 67 mL, 100 mmol). The resulting solution was heated to 80° C. for 6 h before the solvent was evaporated under vacuum. The residue was dissolved in 1.0 M aqueous hydrochloric acid (100 mL), and this was washed with diethyl ether (100 mL twice). The aqueous layer was basified to pH 10 with 50% aqueous sodium hydroxide and extracted with dichloromethane (50 mL three times). The combined dichloromethane extracts were dried (anhydrous sodium sulfate) and evaporated under vacuum to obtain 4-aminomethyl-1-(1-naphthylsulfonyl)piperidine (9.1 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517991B2
Source datasetuspto-grants-2009_04
ORD IDord-96211a1ab580490d902bc8dbc4f521a4
Source noteuspto-grants-2009_04