HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583987Generated: October 31, 2026
Hydrochloric Acid → 4-(1H-imidazol-1-yl)butan-1-amine
https://huagongshe.com/reaction/1583987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 1H-Imidazole-1-hexanamine | HCID 7138477 | — |
| Reactant | N-[4-(imidazol-1-yl)butyl]phthalimide | HCID 13290795 | — |
| Reactant | 7-(1H-imidazol-1-yl)heptan-1-amine | HCID 13952860 | — |
| Reactant | 1H-Imidazole-1-octanamine | HCID 13952861 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(1H-imidazol-1-yl)butan-1-amine | HCID 4379480 | — |
Reaction Steps
A mixture of 0.2 mole of 2-[4-(1H-imidazol-1-yl)butyl]-1H-isoindole-1,3(2H)-dione, 0.22 mole of hydrazine hydrate and 400 ml of ethanol was heated on a steam bath for 3 hours and then treated with 400 ml of 3N hydrochloric acid and then heated at reflux for an additional 2 hours. The insoluble material was filtered off and the mother liquor was concentrated to a low volume and again filtered. The remainder of the volatile material was distilled off and the residue was treated with saturated potassium carbonate solution. The 1H-imidazole-1-butanamine was extracted into methylene chloride and further purified by distillation on a Kugelrohr apparatus. In like manner from the appropriate 2-[ω-(1H-imidazol-1-yl)alkyl]-1H-isoindole-1,3(2H)-diones were prepared 1H-imidazole-1-pentanamine; 1H-imidazole-1-hexanamine; 1H-imidazole-1-heptanamine; and 1H-imidazole-1-octanamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04555519 |
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| Source dataset | uspto-grants-1985_11 |
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| ORD ID | ord-761d985aa6e5403480e77267acf11d11 |
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| Source note | uspto-grants-1985_11 |
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