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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Phenyl-1-propanone | HCID 7148 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | p-Tolyltosylate | HCID 86755453 | — |
| Reactant | 4-Methylphenyl-p-toluene sulfonate | HCID 86755455 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Alpha-(4-methoxyphenyl)propiophenone | HCID 11096728 | 60% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06072073 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-d11e3ff76f1b492dad36cb286a9e7fd2 |
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| Source note | uspto-grants-2000_06 |
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