HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250515Generated: October 25, 2026
4'-Hydroxypropiophenone → 4-Propanoylanisole
https://huagongshe.com/reaction/250515
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4'-Hydroxypropiophenone | HCID 6271 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Propanoylanisole | HCID 67144 | — |
Reaction Steps
To a solution of 4′-hydroxypropiophenone (1.0 g, 6.67 mmol) in acetonitrile (50.0 mL) was added potassium carbonate (7.17 g, 66.7 mmol) and the mixture heated to reflux for 90 min. After this time the reaction mixture was allowed to cool to room temperature and dimethyl sulphate (1.05 mL, 11.1 mmol) was added and the reaction mixture was heated to reflux for a further 19 h. After cooling the acetonitrile was evaporated under reduced pressure and the residue taken up in water and extracted with dichloromethane. The dichloromethane extract was dried (MgSO4) and evaporated under reduced pressure to give 4′-methoxypropiophenone as a yellow oil, (970 mg, 89%) 1H nmr (d6-DMSO, 300 MHz) 1.06, t (7.2 Hz), CH3; 2.95, q (7.2 Hz), CH2; 3.83, s, OMe; 7.02, d (6.9 Hz), H3′,5′; 7.93, d (6.9 Hz), H2′,6′. ESI (+ve) MS m/z 165 (M+H, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863313B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-9c1f92022972431ea749753779867a42 |
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| Source note | uspto-grants-2011_01 |
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