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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506930Generated: October 30, 2026

Water → 1-Boc-4-(aminomethyl)piperidine

https://huagongshe.com/reaction/1506930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 23282921HCID 23282921—
SolventTetrahydrofuranHCID 8028—
Product1-Boc-4-(aminomethyl)piperidineHCID 73681779.1%

Reaction Steps

Tertiary butyl 4-(azidomethyl)piperidine-1-carboxylate (30 g, 124.8 mmol) was dissolved in tetrahydrofuran (300 mL), and triphenylphosphine (39.3 g, 149.8 mmol) was added thereto, followed by stirring under reflux for 2 hours. Water (120 mL) was added thereto, followed by stirring under reflux for another 3 hours and concentration under reduced pressure. The resulting residue was extracted with ethyl acetate and a 1N hydrochloride solution, and the aqueous layer was neutralized with a 2N sodium hydroxide solution, followed by re-extraction with dichloromethane. The resulting organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to afford the title compound (21.16 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221790B2
Source datasetuspto-grants-2015_12
ORD IDord-110b345937664c8e949d4353afba433f
Source noteuspto-grants-2015_12