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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079404Generated: October 30, 2026

Hydrochloric Acid → 1-Tert-butyloxycarbonyl-4-(4-amino-3-methylphenyloxy)piperidine hydrochloride

https://huagongshe.com/reaction/1079404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-butyl 4-(3-methyl-4-nitrophenoxy)piperidine-1-carboxylateHCID 18542679—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-Tert-butyloxycarbonyl-4-(4-amino-3-methylphenyloxy)piperidine hydrochlorideHCID 23366892—

Reaction Steps

To a solution of 1-tert-butyloxycarbonyl-4-(4-nitro-3-methylphenyloxy)piperidine (3.6 g) in ethanol (30 ml) was added conc. hydrochloric acid (0.9 ml). By using 10% palladium/carbon (containing 48% water, 0.3 g) as a catalyst, catalytic reduction was conducted under reduced pressure for 1.5 hours. The catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to obtain 1-tert-butyloxycarbonyl-4-(4-amino-3methylphenyloxy)piperidine hydrochloride (1.7 g) as light brown crystals, m.p. 160°-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580883
Source datasetuspto-grants-1996_12
ORD IDord-e84e5074125b47359766b579fcc246ce
Source noteuspto-grants-1996_12