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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618709Generated: October 29, 2026

Ammonium Chloride → HCID 15434546, compound

https://huagongshe.com/reaction/618709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium BicarbonateHCID 516892—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
ReactantHCID 15434545HCID 15434545—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 15434546HCID 1543454640%

Reaction Steps

A mixture of 1.4 g (7.1 mmol) of 5,6-difluorobenzofuran-2-carboxamide and 1.62 g (8.5 mmol) of triethyloxonium tetrafluoroborate in 40 ml of anhydrous dichloromethane was stirred at room temperature over 64 hours. Subsequently, the mixture was poured into 70 ml of saturated sodium hydrogen carbonate solution, extracted twice with 100 ml of dichloro-methane each time and the combined organic phases were washed once with 70 ml of saturated sodium hydrogen carbonate solution, dried over magnesium sulfate and concentrated in a vacuum. The brown solid obtained was dissolved in 30 ml of anhydrous ethanol, treated with 2 g of ammonium chloride and heated under reflux for 22 hours. The mixture was diluted with 90 ml of ethyl acetate and extracted three times with 50 ml of water each time. Subsequently, the combined aqueous phases were made basic with 3N sodium hydroxide solution and the solid was filtered off and washed with water. After drying there was obtained 0.55 g (40%) of 5,6-difluorobenzofuran-2-carboxamidine as a white solid with m.p. 178°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05955495
Source datasetuspto-grants-1999_09
ORD IDord-9870f8c057264c43a398d76a4b9090d1
Source noteuspto-grants-1999_09