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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908880Generated: October 26, 2026

4'-Fluoroacetophenone → Ethanone, 1-[4-(4-ethyl-1H-imidazol-1-yl)phenyl]-

https://huagongshe.com/reaction/908880

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-FluoroacetophenoneHCID 9828—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178437183HCID 178437183—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthanone, 1-[4-(4-ethyl-1H-imidazol-1-yl)phenyl]-HCID 45095120—

Reaction Steps

NaH (0.068 g in 60% oil dispersion, 1.7 mmol) was added to a solution of compound 16 (0.180 g, 1.8 mmol) in DMF (6 mL) with stirring at room temperature. The mixture was stirred for 15 min and a solution of 4′-fluoroacetophenone (0.215 g, 1.56 mmol) in DMF (2 mL) was added. The reaction mixture was heated at 80° C. for 1 h, and then cooled, diluted with water, and extracted with EtOAc. The organic layer was washed with brine, dried, and evaporated to a yellow solid. Compound 17 crystallized to form white color needles upon standing at room temperature. The yield was 0.270 g, 67%. The structure was confirmed by 1H NMR in CDCl3. LC-MS: [M+1]=215. Purity was >98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017629B2
Source datasetuspto-grants-2011_09
ORD IDord-a2d57e49f5c44b90a2d91fafadd99227
Source noteuspto-grants-2011_09