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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877010Generated: October 29, 2026

Acetophenone → Phenacyl bromide

https://huagongshe.com/reaction/877010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
ReactantBromineHCID 24408—
SolventAcetic AcidHCID 176—
ProductPhenacyl bromideHCID 6259—

Reaction Steps

Synthesis of 2-amino-4-arylimidazolamine of the formula (48) (wherein R4, R5, R6, R7 R8 and R9 are as defined above) is described in Scheme 9. Thus, reaction of acetophenone derivative of formula (45) with bromine in acetic acid gives phenacyl bromide, which on reaction with acetyl guanidine in acetonitrile at reflux temperature gives N-acetyl imidazole of the formula (47). The N-deacetylation of (47) under acidic conditions affords 2-amino-4-arylimidazoles of the formula (48). This is similar to the procedure reported by Thomas, L. et al in J. Org. Chem., 1994, 59, 7299-7305.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987278B2
Source datasetuspto-grants-2015_03
ORD IDord-d4c12c3bc1bc40b880395d771cb47b98
Source noteuspto-grants-2015_03