HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 494925Erstellt: 25. Oktober 2026
Methyl iodide → 2'-Hydroxy-4'-methoxypropiophenone
https://huagongshe.com/reaction/494925
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2',4'-Dihydroxypropiophenone | HCID 79856 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | 2'-Hydroxy-4'-methoxypropiophenone | HCID 234836 | 86,7% |
Reaktionsschritte
6.00 g of 2′,4′-dihydroxypropiophenone was dissolved in 70 ml of acetone. Thereafter, 7.09 g of potassium carbonate and 3.03 ml of methyl iodide were successively added to the reaction solution. The reaction solution was then heated to reflux. Approximately 3 hours later, the reaction solution was stood to cool and then filtered. The filtrate was concentrated under a reduced pressure. A saturated sodium chloride solution and ethyl acetate were added to the residue, so as to separate an organic layer. The obtained organic layer was washed with 2 N hydrochloric acid and a saturated sodium chloride solution, and then dried over anhydrous magnesium sulfate. After removing the drying agent by filtration, the organic layer was concentrated under a reduced pressure. The residue was solidified from hexane-ethyl acetate, so as to obtain 5.64 g of the subject compound. 1H-NMR (CDCl3) δ (ppm): 1.23 (t, J=7.2 Hz, 3H), 2.95 (q, J=7.2 Hz, 2H), 3.83 (s, 3H), 6.40-6.45 (m, 2H), 7.65 (dd, J=1.6 Hz, 8.0 Hz, 1H), 12.8 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07538123B2 |
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| Quelldatensatz | uspto-grants-2009_05 |
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| ORD ID | ord-960c7f38786941e9982a2744e0c1e361 |
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| Quellennotiz | uspto-grants-2009_05 |
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