HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618709Generated: October 29, 2026
Ammonium Chloride → HCID 15434546, compound
https://huagongshe.com/reaction/618709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Reactant | HCID 15434545 | HCID 15434545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 15434546 | HCID 15434546 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05955495 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-9870f8c057264c43a398d76a4b9090d1 |
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| Source note | uspto-grants-1999_09 |
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