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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258150Generated: October 26, 2026

Trifluoroacetic acid → 1-(3,4,5-Trifluoro-benzyl)-piperidin-4-ylamine

https://huagongshe.com/reaction/1258150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Reactant3,4,5-Trifluorobenzyl bromideHCID 2777062—
SolventDichloromethaneHCID 6344—
Product1-(3,4,5-Trifluoro-benzyl)-piperidin-4-ylamineHCID 53256189105.1%

Reaction Steps

A mixture of piperidin-4-ylcarbamic acid tert-butyl ester (2.5 g, 12.4 mmol), 3,4,5-trifluorobenzyl bromide (2.5 g, 11.3 mmol) and diisoproylethylamine (2.9 ml, 16.9 mmol) in dichloromethane (25 ml) was stirred at room temperature for 2 h. After this period, trifluoroacetic acid (15.6 ml) was added and the reaction was stirred for a further 2 h. The solvent was evaporated in vacuo and a saturated solution of sodium carbonate was added. The mixture was extracted with dichloromethane and the separated organic layers were dried (Na2SO4), filtered, and the solvent evaporated in vacuo to yield D8 (2.9 g, 96%) as a solid. C12H15F3N2 requires 244. Found 245 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466153B2
Source datasetuspto-grants-2013_06
ORD IDord-db277315753a4a08b644d327092ada98
Source noteuspto-grants-2013_06