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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258147Generated: October 30, 2026

Trifluoroacetic acid → 1-[(3,5-Difluorophenyl)methyl]piperidin-4-amine

https://huagongshe.com/reaction/1258147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylethylamineHCID 81531—
Reactant3,5-Difluorobenzyl bromideHCID 518896—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
SolventDichloromethaneHCID 6344—
Product1-[(3,5-Difluorophenyl)methyl]piperidin-4-amineHCID 2218240090%

Reaction Steps

A mixture of piperidin-4-ylcarbamic acid tert-butyl ester (5 g, 24.9 mmol), 3,5-difluorobenzyl bromide (2.9 ml, 22.7 mmol) and diisoproylethylamine (5.9 ml, 34.03 mmol) in dichloromethane (50 ml) was stirred at room temperature for 2 h. After this period, trifluoroacetic acid (32 ml) was added and the reaction mixture 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 D5 (4.5 g, 90%) as a solid. C12H16F2N2 requires 226. Found 227 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466153B2
Source datasetuspto-grants-2013_06
ORD IDord-ecc59bcfadf046a190ad4b58c8285c18
Source noteuspto-grants-2013_06