HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443537Generated: October 29, 2026
Benzamidine, hydrochloride → HCID 178477950, compound
https://huagongshe.com/reaction/1443537
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzamidine, hydrochloride | HCID 80289 | — |
| Reactant | 2-Bromo-1-(3,4-dichlorophenyl)ethanone | HCID 244751 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178477950 | HCID 178477950 | — |
Reaction Steps
A solution of 68.0 g (0.254 mol) of the above-mentioned crude 2-bromo-3′,4′-dichloroacetophenone in 110 ml of tetrahydrofuran was added dropwise over 30 minutes, under reflux with heating, into a suspension of 39.8 g (0.254 mol) of benzamidine hydrochloride, 102.1 g (1.02 mol) of potassium bicarbonate in 400 ml of tetrahydrofuran and 100 ml of water. After the addition was complete, further refluxing with heating was carried out for 2 hours. The reaction solution was evaporated to dryness under reduced pressure, to give a residual solid. This solid was successively washed with water and toluene, to give 45.5 g (62.0% crude yield) of crude crystals of the desired product. The crude crystals were recrystallized using acetonitrile, to give a purified white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07661577B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-4ce33d2532c2474581d5dea9658dc687 |
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| Source note | uspto-grants-2010_02 |
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