Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485088Generated: November 1, 2026

1-(4-Biphenyl)-1-propanol → p-Phenylpropiophenone

https://huagongshe.com/reaction/1485088

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Biphenyl)-1-propanolHCID 13130482—
CatalystHCID 178418406HCID 178418406—
SolventDiethyl EtherHCID 3283—
Productp-PhenylpropiophenoneHCID 9523073.2%

Reaction Steps

To a solution in diethyl ether (30.0 mL) of the compound (1.27 g) obtained in step (1) above, manganese(IV) oxide (9.57 g) was added and the mixture was stirred at room temperature for 45 hours. After removing the insoluble matter by filtration, the filtrate was concentrated under reduced pressure. To a solution of the resulting residue in acetone (60.0 mL), a Jones' reagent {see Org. Synth., Coll. Vol. VI, 542 (1988)}(1.20 mL) was added until the color of the Jones' reagent was yet to disappear. The reaction mixture was concentrated under reduced pressure and ethyl acetate and water were added to the residue. Extraction with ethyl acetate was conducted three times and the combined organic layers were washed with saturated brine. After passage through a phase separator, the washed organic layers were concentrated under reduced pressure. The resulting residue was recrystallized with n-hexane to give the titled compound as a colorless solid (921 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422240B2
Source datasetuspto-grants-2016_08
ORD IDord-fa03332dda2e4c59880616176888c9fe
Source noteuspto-grants-2016_08