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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421112Generated: November 1, 2026

1-Phenyl-1-propanone → Alpha-(4-methoxyphenyl)propiophenone

https://huagongshe.com/reaction/1421112

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenyl-1-propanoneHCID 7148—
ReactantSodium t-butoxideHCID 23676156—
Reactantp-TolyltosylateHCID 86755453—
Reactant4-Methylphenyl-p-toluene sulfonateHCID 86755455—
Catalystpalladium(II) acetateHCID 167845—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
ProductAlpha-(4-methoxyphenyl)propiophenoneHCID 1109672860%

Reaction Conditions

Temperature100 °C

Reaction Steps

Reaction of propiophenone with p-tolyltosylate: Pd(OAc)2 (9.0 mg, 0.040 mmol), ligand (27.1 mg, 0.050 mmol), NaOtBu (144 mg, 1.50 mmol) and 4-methylphenyl-p-toluene sulfonate (262 mg, 1.00 mmol) were suspended in 1 mL of dioxane in a screw-capped vial. The vial was sealed with a cap containing a PTFE septum and removed from the dry box. Propiophenone (132 mg, 1.10 mmol) was added to the reaction mixture by syringe. The reaction mixture was stirred at 100° C. and monitored by GC analysis. The crude reaction was diluted with ether and washed with 1N HCl, water and brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The residue was chromatographed on silica gel (hexane/EtOAc=95/5) to give 135 mg (60%) of 2-(4-Methoxyphenyl)-1-phenyl-1-propanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06072073
Source datasetuspto-grants-2000_06
ORD IDord-d11e3ff76f1b492dad36cb286a9e7fd2
Source noteuspto-grants-2000_06