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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972749Generated: October 29, 2026

4-Hydroxybiphenyl → 1-([1,1′-Biphenyl]-4-yloxy)-3,3-dimethyl-2-butanone

https://huagongshe.com/reaction/972749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybiphenylHCID 7103—
ReactantPotassium CarbonateHCID 11430—
Reactant1-ChloropinacoloneHCID 83572—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-ChloropinacoloneHCID 83572—
Product1-([1,1′-Biphenyl]-4-yloxy)-3,3-dimethyl-2-butanoneHCID 23050426163.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

510 g (3 moles) of 4-hydroxybiphenyl were dissolved in 3 l of methyl ethyl ketone. 390 g of ground potassium carbonate were added and the mixture was heated to 80° C. 405 g (3 moles) of α-chloropinacoline were added dropwise over the course of 2 hours and the mixture was then stirred for a further 15 hours at 80° C. After cooling, it was filtered and the filter residue was rinsed with methyl ethyl ketone. The resulting filtrate was concentrated to dryness in vacuo by distilling off the solvent. The residue was taken up in methylene chloride and the solution was washed with 10% strength sodium hydroxide solution and twice with water, dried over sodium sulfate and concentrated in vacuo by distilling off the solvent. The residue was distilled, using a condenser cooled with hot water (50° C.), to avoid crystallization. After a small amount of first runnings of chloropinacoline at 40° C./0.4 mm Hg, 658 g (82% of theory) of 1-(4'-phenyl-phenoxy)3,3-dimethylbutan-2-one were obtained at 170° to 180° C./0.4 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04053616
Source datasetuspto-grants-1977_10
ORD IDord-4a28c052a6754287ad514d3944644805
Source noteuspto-grants-1977_10