HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544408Generated: November 1, 2026
Hydrochloric Acid → HCID 178507226, compound
https://huagongshe.com/reaction/544408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178526429 | HCID 178526429 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178507226 | HCID 178507226 | 87.2% |
Reaction Steps
A solution of concentrated hydrochloric acid (2.8 ml, 0.028 M) in aqueous ethanol (50%, 15 ml) was added dropwise to a stirred heated mixture of 2-(2,6-dibromo-4-nitro phenylimino)imidazolidine (4 g, 0.011 M) and iron powder (1.9 g, 0.034 M) in aqueous ethanol (50%). The mixture was heated under reflux for 3 hours after which time it was filtered hot and evaporated to a low volume. This residual solution was acidified with dilute hydrochloric acid and the resulting solid was removed. The solutionwas then basified with dilute aqueous sodium hydroxide yielding a solid which was collected. This solid was triturated with hot methanol which wasthen evaporated to leave a brown solid (3.2 g). This solid was chromatographed on alumina and eluted with a methanol in methylene chloride gradient. The fractions containing the required compound were combined and evaporated affording 2-(4-amino-2,6-dibromophenylimino)imidazoline dihydrochloride, mp>320° C. (1.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04450170 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-4c18d10fdeca402a8d26d6a4a84163b2 |
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| Source note | uspto-grants-1984_05 |
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