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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193336Generated: October 31, 2026

Trifluoroacetic acid → N-Benzyl-N-methyl-2-(piperidin-4-yl)ethanamine

https://huagongshe.com/reaction/1193336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 4-(2-(benzyl(methyl)amino)ethyl)piperidine-1-carboxylateHCID 19261850—
SolventDichloromethaneHCID 6344—
ProductN-Benzyl-N-methyl-2-(piperidin-4-yl)ethanamineHCID 19085399—

Reaction Steps

TFA (2.78 ml) was added dropwise at 0° C. to a solution of tert-butyl 4-(2-(benzyl(methyl)-amino)ethyl)piperidine-1-carboxylate (600 mg, 1.8 mmol, 1 eq) in dichloromethane (30 ml), and stirring was carried out for 1 h at RT. After monitoring by thin-layer chromatography, the reaction mixture was concentrated to dryness. The residue was dissolved in MeOH (50 ml), Amberlyst A-21 ion-exchanger resin (2 g) was added, and stirring was carried out for 30 min. The reaction mixture was filtered and the filtrate was concentrated to dryness under reduced pressure and used in the next stage without being purified further.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-2e3ef4c773794b22ae3c39085d0739a8
Source noteuspto-grants-2014_03