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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101504Generated: October 30, 2026

HCID 57801503, compound → HCID 57801504, compound

https://huagongshe.com/reaction/2101504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57801503HCID 57801503—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
SolventIronHCID 23925—
ProductHCID 57801504HCID 5780150490%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572921B2
Source datasetuspto-grants-2009_08
ORD IDord-afef5cfc9a73491389aee36cd93cffc2
Source noteuspto-grants-2009_08