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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367836Generated: November 2, 2026

Phenacyl bromide → HCID 178474414, compound

https://huagongshe.com/reaction/1367836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantHCID 178475102HCID 178475102—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178474414HCID 178474414—

Reaction Steps

To a solution of 2.0 g (10 mmol) of 2-bromoacetophenone in DMF (30 mL) was added 3.0 g (29 mmol) 1-acetylguanidine in one portion, the reaction mixture was stirred at rt for 2 days. The reaction mixture was diluted with EtOAc (250 mL) and washed with saturated NH4Cl aq. solution (50 mL). The organic phase was dried over MgSO4 and concentrated under vacuum. The residue was purified by a flash column chromatography eluting with EtOAc to give N-(4-phenyl-1H-imidazol-2-yl)-acetamide. (0.5 g, 24%). LCMS: 203 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893267B2
Source datasetuspto-grants-2011_02
ORD IDord-b4bae55fc8414f109c534a56b0c32ed6
Source noteuspto-grants-2011_02