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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907368Generated: October 31, 2026

Triethylamine → HCID 24700958, compound

https://huagongshe.com/reaction/1907368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
ReactantIsobutyl chloroformateHCID 62365—
Reactant6-Chloronicotinic acidHCID 79222—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 24700958HCID 2470095867.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (1.03 ml, 7.4 mmol) and isobutyl chloroformate (0.76 ml, 5.5 mmol) were added to an acetonitrile solution (12 ml) of 6-chloronicotinic acid (0.58 g, 3.6 mmol) under ice cooling and the mixture was stirred at 0° C. for 30 minutes. To the solution mixture, 2,2,2-trifluoroethyl amine (0.88 ml, 11.2 mmol) was added and the mixture was stirred at room temperature for 10 minutes. Water was added to the reaction solution, which was then extracted with ethyl acetate. The extraction solution with ethyl acetate was dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (n-hexane:ethyl acetate=5:1→1:1). The purified product was concentrated under reduced pressure and diisopropyl ether and n-hexane were added. The insoluble matter precipitated was obtained by filtration and dried to obtain 6-chloro-N-(2,2,2-trifluoroethyl)nicotine amide (0.58 g) as light yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598162B2
Source datasetuspto-grants-2013_12
ORD IDord-3ac5f1f36c29460d9a037daac2348571
Source noteuspto-grants-2013_12