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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856657Generated: October 25, 2026

Triethylamine → N-(4-nitrobenzyl)trifluoroacetoamide

https://huagongshe.com/reaction/856657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,2,2-Trifluoroethyl AcetateHCID 136256—
Reactant4-Nitrobenzylamine hydrochlorideHCID 11252467—
SolventAcetonitrileHCID 6342—
ProductN-(4-nitrobenzyl)trifluoroacetoamideHCID 14317262—

Reaction Steps

To a suspension of 4-nitrobenzylamine hydrochloride (10.0 g) and triethylamine (22.2 ml) in acetonitrile (100 ml) was added trifluoroethyl acetate (12.6 ml) at room temperature and the mixture was stirred for 24 hours. The solvent was removed under reduced pressure, water was added to the mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate and concentrated under reduced pressure. The precipitated crystals were collected by filtration. The crystals were washed with hexane, to give N-(4-nitrobenzyl)trifluoroacetoamide (12.79 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262185B2
Source datasetuspto-grants-2007_08
ORD IDord-2b75692cde864675be581d7fbd123640
Source noteuspto-grants-2007_08