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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17887Generated: October 25, 2026

3-Hydroxyacetophenone → 1-[3-(3-Phenylpropoxy)phenyl]ethan-1-one

https://huagongshe.com/reaction/17887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxyacetophenoneHCID 8487—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Bromopropyl)benzeneHCID 12503—
CatalystSodium IodideHCID 5238—
SolventDimethylformamideHCID 6228—
Product1-[3-(3-Phenylpropoxy)phenyl]ethan-1-oneHCID 2142244094.4%

Reaction Steps

3′-Hydroxyacetophenone (6.81 g, 50 mmol) and 1-bromo-3-phenyl propane (11.95 g, 60 mmol) were dissolved in dimethylformamide (70 ml). Then, potassium carbonate (15 g) and sodium iodide (0.5 g) were added thereto and the mixture was allowed to react for 7 hours at 80° C. Ethyl acetate (300 ml) and purified water (200 ml) were further added to the reaction mixture prior to stirring for 30 min. The organic layer extracted with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:5) to obtain the title compound (12.0 g, yield 94.2%) as a gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741323B2
Source datasetuspto-grants-2010_06
ORD IDord-4521dbc84ec14ce1a4ca820a0481d911
Source noteuspto-grants-2010_06