Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978342Generated: October 28, 2026

Triethylamine → N-(1-tert-butoxycarbonylpiperidin-4-ylmethyl)trifluoroacetamide

https://huagongshe.com/reaction/1978342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl trifluoroacetateHCID 9794—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
SolventAcetonitrileHCID 6342—
ProductN-(1-tert-butoxycarbonylpiperidin-4-ylmethyl)trifluoroacetamideHCID 2199402087%

Reaction Steps

To a solution of 5.07 g (23.7 mM) of tert-butyl 4-aminomethylpiperidine-1-carboxylate and 5.0 ml (35.9 mM) of triethylamine in acetonitrile (40 ml) was added 5.6 ml (47.1 mM) of ethyl trifluoroacetate at room temperature and the mixture was stirred at room temperature for 1.5 hours. After the solvent was distilled off under reduced pressure, the residue was diluted with ethyl acetate and washed with water and saturated aqueous solution of sodium chloride. The solvent was then distilled off under reduced pressure to provide the title compound as light-yellow solid (6.40 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235731B1
Source datasetuspto-grants-2001_05
ORD IDord-2b40047e704b46ddb68aba63759d5e5d
Source noteuspto-grants-2001_05