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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499191Generated: October 26, 2026

N-Boc-3-[(1-Cbz-4-piperidyl)oxy]aniline → 1-Cbz-4-(3-aminophenoxy)-piperidine

https://huagongshe.com/reaction/499191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Boc-3-[(1-Cbz-4-piperidyl)oxy]anilineHCID 68454608—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product1-Cbz-4-(3-aminophenoxy)-piperidineHCID 68453441—

Reaction Conditions

Temperature22 °C

Reaction Steps

4-(3-tert-Butoxycarbonylamino-phenoxy)-piperidine-1-carboxylic acid benzyl ester (11.8 g, 27.6 mmol) is dissolved in a solution of trifluoroacetic acid in dichloromethane (25% v/v, 20 mL). The reaction mixture is stirred at 22° C. for 60 min. After removal of the solvent, the oily residue is dissolved in dichloromethane (250 mL) and neutralized with 0.2 N aqueous sodium hydroxide solution (250 mL) and extracted with dichloromethane (10×100 mL) followed by ethyl acetate (5×100 mL). The combined organic phases are dried over anhydrous sodium sulfate. After removal of solvent, the crude product is purified on silica gel chromatography with dichloromethane-methanol to give a light brown oil (4.84 g, 54%, ES+(m/z) 327.3 [M+H]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767674B2
Source datasetuspto-grants-2010_08
ORD IDord-1423ec6a4ad149ad98a04e0a774cde5c
Source noteuspto-grants-2010_08