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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626501Generated: October 30, 2026

Hydrochloric Acid → HCID 67287673, compound

https://huagongshe.com/reaction/1626501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant(2E)-3-Ethoxy-2-propenenitrileHCID 5324714—
ReactantSodiumHCID 5360545—
Reactant(3,4-Difluorophenyl)hydrazine--hydrogen chloride (1/1)HCID 24721344—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 67287673HCID 6728767323.1%

Reaction Steps

To ethanol (28 ml) was added sodium (0.407 g, 17.7 mmol), and the mixture was stirred about 30 minutes. To this, (3,4-difluorophenyl)hydrazine hydrochloride (1.00 g, 5.54 mmol) and (E)-3-ethoxyacrylonitrile (0.912 ml, 8.86 mmol) were added, and the reaction was heated to reflux for 16 hours. The reaction was diluted with water (30 ml) and acidified to pH 3 with 5M hydrochloric acid. The reaction was allowed to stir at ambient temperature for another 2 hours and was then neutralized (pH 7) by the addition of 5M sodium hydroxide. The reaction was concentrated to remove most of the ethanol. The resulting suspension was extracted twice with EtOAc, and the combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product was purified by silica gel chromatography, eluting with a linear gradient of 20-100% EtOAc/hexanes to yield the desired product (0.250 g, 1.28 mmol, 23.1% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785445B2
Source datasetuspto-grants-2014_07
ORD IDord-02d955df87724f3981c77a3c54c0e4c8
Source noteuspto-grants-2014_07