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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Trifluoromethyl)aniline | HCID 6922 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-Butyl 4-((2-(trifluoromethyl)phenyl)amino)piperidine-1-carboxylate | HCID 66591750 | 95.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951805B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-7209266d3441434db6eb2158da4c08e3 |
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| Source note | uspto-grants-2011_05 |
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