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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552129Generated: October 28, 2026

tert-Butyl 4-((2-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate → Piperidin-4-yl-(2-trifluoromethylphenyl)amine

https://huagongshe.com/reaction/552129

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-((2-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylateHCID 66591750—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductPiperidin-4-yl-(2-trifluoromethylphenyl)amineHCID 5490268299.4%

Reaction Steps

A solution of 4-(2-trifluoromethylphenylamino)piperidine-1-carboxylic acid tert-butyl ester (0.87 g, 2.52 mmol) in dichloromethane and trifluoroacetic acid (18 mL, 2:1) was stirred at ambient temperature overnight, the solvents were removed by evaporation. The residue was dissolved in ethyl acetate, and the resulting solution was washed with aqueous saturated NaHCO3 and brine, dried over anhydrous Na2SO4 and concentrated to give piperidin-4-yl-(2-trifluoromethylphenyl)amine (0.612 g, 99%) which was used directly for next step reaction without further purification. MS (ES+) m/z 245.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951805B2
Source datasetuspto-grants-2011_05
ORD IDord-44bf684b51304b46bea8dd1d5d60d737
Source noteuspto-grants-2011_05