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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229345Generated: October 31, 2026

Ethylamine → HCID 18466607, compound

https://huagongshe.com/reaction/2229345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantPhenyl triflimideHCID 142176—
ReactantHCID 10750851HCID 10750851—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 18466607HCID 1846660741%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 3-nitro-6-(trifluoromethyl)-2(1H)-pyridinone (2.4 g, 11.5 mmol) in DMF (69 mL) was added sodium hydride (350 mg, 13.8 mmol). The reaction was stirred for 30 min at 45° C., cooled to room temperature and N-phenyltrifluromethanesulfonimide (4.9 g, 13.8 mmol) was added. After 1 h, a 2 M solution of ethylamine in THF (13 mL, 25 mmol) was added. The reaction was stirred at room temperature overnight. The reaction mixture was poured into water (100 mL) and extracted with EtOAc (3×). The combined organic layer was successively washed water and brine, dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (hexane:EtOAc, 9:1) to give the desired compound (1.1 g, 41% yield) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420359B1
Source datasetuspto-grants-2002_07
ORD IDord-c7f0614c755e478d96c844e241c18e90
Source noteuspto-grants-2002_07