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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025662Generated: November 3, 2026

Ammonia → HCID 178512013, compound

https://huagongshe.com/reaction/1025662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantSodium BicarbonateHCID 516892—
Reactant2,4-dichloro-N-(4-(trifluoromethyl)phenyl)benzamideHCID 956453—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178512013HCID 17851201389%

Reaction Conditions

Temperature0 °C

Reaction Steps

Part B: 2,4-Dichloro-N-(4-(trifluoromethyl)phenyl)benzamide (19.0 g, 0.057 mol) is dissolved in benzene (150 mL) and PCl5 (13.0 g, 1.1 molar equivalent) is added. The resulting mixture is heated at reflux temperature for two hours, allowed to attain room temperature and concentrated in vacuo to give a residue. The residue is dissolved in anhydrous THF, cooled to 0° C. and transferred into an autoclave. Excess NH3 is quickly added from a lecture bottle and the mixture is stirred at room temperature for 50 hours. A mixture of ethylacetate and aqueous NaHCO3 is added. The ethylacetate layer is collected, dried over Na2SO4, filtered and concentrated in vacuo. The resulting oil is purified by column chromatography (diethyl ether/petroleum ether=1/1 (v/v), silicagel) to give pure 2,4-dichloro-N-(4-(trifluoromethyl)phenyl)benzene-carboxamidine (16.9 g, 89% yield). Melting point: 108-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729101B2
Source datasetuspto-grants-2014_05
ORD IDord-cd3909ae8c4c42849ce9afeb6e1042de
Source noteuspto-grants-2014_05