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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459175Generated: October 29, 2026

Acetone → 4-[(Prop-2-en-1-yl)oxy]-1,1'-biphenyl

https://huagongshe.com/reaction/459175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant4-HydroxybiphenylHCID 7103—
ReactantPotassium CarbonateHCID 11430—
Product4-[(Prop-2-en-1-yl)oxy]-1,1'-biphenylHCID 257986—

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of 4-phenylphenol (1 eq) in acetone, K2CO3 (2 eq) and alkyl bromide (1.2 eq) were added and the mixture reaction was stirred at 55° C. overnight. Quenched with water and extracted with ethyl acetate. The organic layer was dried (MgSO4) and concentrated to give 4-allyloxybiphenyl. This crude product was dissolved in Me2NPh and heated to reflux for 6 hours and then stirred at room temperature over 3 days. Refluxed again for 8 hours and then poured into and ice-cold HCl 1M solution, extracted with ethyl acetate and washed with water. Dried and concentrated to give a crude product which was purified by chromatography to give the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192982B2
Source datasetuspto-grants-2007_03
ORD IDord-878d0cf0f3354885bd4f201d046954ab
Source noteuspto-grants-2007_03