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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552128Generated: October 29, 2026

2-(Trifluoromethyl)aniline → tert-Butyl 4-((2-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate

https://huagongshe.com/reaction/552128

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethyl)anilineHCID 6922—
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium cyanoborohydrideHCID 5003444—
CatalystTitanium isopropoxideHCID 11026—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-((2-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylateHCID 6659175095.2%

Reaction Steps

Titanium isopropoxide (2.5 mL, 8.46 mmol) was added to a solution of 2-aminobenzotrifluoride (0.6 mL, 4.82 mmol) and 1-Boc-4-piperidone (1.05 g, 5.26 mmol)) in THF (3 mL), the resulting mixture was stirred at ambient temperature for 4 hours, then sodium cyanoborohydride (0.800 g, 12.73 mmol) was added. The stirring was continued overnight. Aqueous sodium hydroxide (2.0 mL, 1.0 M) was added and the mixture was stirred for another 15 minutes. The reaction mixture was diluted with ethyl acetate (250 mL), washed with water, and brine, dried over anhydrous Na2SO4, and concentrated. The residue was purified by flash chromatography to afford 4-(2-trifluoromethylphenylamino)piperidine-1-carboxylic acid tert-butyl ester (1.58 g, 95%). MS (ES+) m/z 345.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951805B2
Source datasetuspto-grants-2011_05
ORD IDord-7209266d3441434db6eb2158da4c08e3
Source noteuspto-grants-2011_05