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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43348Generated: October 28, 2026

3-(Trifluoromethyl)aniline → 1-Boc-4-(3-trifluoromethyl-phenylamino)-piperidine

https://huagongshe.com/reaction/43348

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
Product1-Boc-4-(3-trifluoromethyl-phenylamino)-piperidineHCID 372233099.9%

Reaction Steps

A Solution of 1,1-Dimethylethyl 4-Oxo-1-Piperidinecarboxylate (0.5 g, 2.5 mmol), 3-(trifluoromethyl)aniline (0.402 g, 2.5 mmol) and sodium tri(acetoxy)borohydride (0.80 g, 3.75 mmol) in 1,2-DCE (5 ml) was stirred at room temperature, under argon overnight. Saturated aq. NaHCO3 solution (15 ml) was added and stirring continued for 1 h. The reaction mixture was extracted with DCM and the organic phase concentrated in vacuo. Recrystallisation of the solid residue gave the title compound as a white solid (0.86 g). δH (CDCl3, 250 MHz)) 7.25 (1H, t), 6.92 (1H, d), 6.75 (2H, m), 4.06 (2H, m), 3.45 (1H, m), 2.94 (2H, m), 2.04 (2H, m), 1.46 (9H, s), 1.36 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536182B2
Source datasetuspto-grants-2013_09
ORD IDord-0341eb119a7e42ef945e757759224d7c
Source noteuspto-grants-2013_09