HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659542Generated: November 1, 2026
Hydrochloric Acid → 5-(4-Bromophenyl)-5-phenylimidazolidine-2,4-dione
https://huagongshe.com/reaction/1659542
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Bromobenzophenone | HCID 7030 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(4-Bromophenyl)-5-phenylimidazolidine-2,4-dione | HCID 13019272 | — |
Reaction Steps
In a 500 ml steel bomb, 60 gr of 4-bromobenzophenone in 300 ml of dimethylformamide, 100 gr of solid ammonium carbonate and 30 gr of potassium cyanide in 100 ml of water are added. After closing the bomb, the reaction mixture is heated to 120° C. for 5 days, then poured under fast mechanical stirring into 2 l of water at 80° C., then acidified (concentrated HCl) and centrifuged after cooling in an ice-bath. A crude product is obtained, which is treated with 2 N sodium hydroxide (500 ml). The suspension is filtered; the filtrate is extracted three times with ether (total of 300 ml). The aqueous phase is acidified with concentrated hydrochloric acid to give 59 gr of 5-(parabromophenyl)-5-phenylhydantoin as a crude product. A recrystallization from ethanol gives 40 gr of pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04304782 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-9038b4bc1b714c759acf463975b4a06b |
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| Source note | uspto-grants-1981_12 |
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