HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101504Generated: October 30, 2026
HCID 57801503, compound → HCID 57801504, compound
https://huagongshe.com/reaction/2101504
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57801503 | HCID 57801503 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Iron | HCID 23925 | — |
| Product | HCID 57801504 | HCID 57801504 | 90% |
Reaction Steps
1-(3,5-dichloro-benzyl)-2-nitro-1H-imidazole was dissolved in a mixture of ethanol and acetic acid, and Fe was added. The mixture was heated to 80° C. for 20 min. During this period of time, the mixture turned into reddish brown in color and then grayish white precipitate was formed. The reaction mixture was cooled to room temperature and diluted with EtOAc. The slurry was filtered through a pad of diatomaceous earth and washed with EtOAc. The filtrate was basified using 2N NaOH solution until pH ˜8. The organic phase was then separated and the aqueous layer was extracted with EtOAc. The combined EtOAc layer was dried over Na2SO4 and concentrated to afford 1-(3,5-dichloro-benzyl)-1H-imidazol-2-ylamine as a white solid (80 mg, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572921B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-afef5cfc9a73491389aee36cd93cffc2 |
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| Source note | uspto-grants-2009_08 |
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