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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272097Generated: October 30, 2026

Hydrochloric Acid → tert-Butyl (3R)-3-(aminomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/272097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriphenylphosphineHCID 11776—
Reactant(S)-Tert-butyl 3-(azidomethyl)piperidine-1-carboxylateHCID 10083012—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl (3R)-3-(aminomethyl)piperidine-1-carboxylateHCID 150202392.9%

Reaction Steps

To a solution of 600 mg of (3S)-3-azidomethyl-1-(tert-butoxycarbonyl)piperidine in 12.5 ml of 20% hydrous tetrahydrofuran, 622 mg of triphenylphosphine was added at room temperature, followed by 45 minutes' refluxing under heating. The reaction liquid was rendered acidic by addition of 0.5 N hydrochloric acid, and successively washed with chloroform and ethyl acetate. Then 4N aqueous sodium hydroxide solution was added to the aqueous layer to render the latter basic, followed by extraction with chloroform and drying over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, 497 mg of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452908B2
Source datasetuspto-grants-2008_11
ORD IDord-607e516fc46f44798928a6187dc4c104
Source noteuspto-grants-2008_11