HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443541Generated: October 29, 2026
Benzamidine, hydrochloride → HCID 23103026, compound
https://huagongshe.com/reaction/1443541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzamidine, hydrochloride | HCID 80289 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 2-Bromo-1-(3,4-dichlorophenyl)propan-1-one | HCID 13435362 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23103026 | HCID 23103026 | — |
Reaction Steps
A solution of 86.6 g (0.307 mol) of the above-mentioned crude 2-bromo-3′,4′-dichloropropiophenone in 120 ml of tetrahydrofuran was added dropwise over 40 minutes into a suspension, under reflux with heating, of 48.1 g (0.307 mol) of benzamidine hydrochloride, 123.4 g (1.23 mol) of potassium bicarbonate in 450 ml of tetrahydrofuran and 110 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 65.3 g (71.3% 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-47b2d3aab91742729d1545a58d8f1383 |
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| Source note | uspto-grants-2010_02 |
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