Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Diethyl Carbonate | HCID 7766 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2'-Hydroxy-4'-methylacetophenone | HCID 81338 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4-Hydroxy-7-methylcoumarin | HCID 54685307 | — |
Reaktionsschritte
To a mechanically stirred suspension of sodium hydride (60% in oil, 30 g, 749 mmol) in toluene (400 mL), heated at 80° C., a solution of the commercially available 2′-hydroxy-4′-methylacetophenone (50 g, 0.333 mmol) in 150 mL of toluene was added dropwise over 1 h. After complete addition, the mixture was stirred 15 min and a solution of diethyl carbonate (81 mL, 666 mmol) in toluene (500 mL) was added dropwise over 1 h. The reaction mixture was then stirred overnight at reflux. After cooling, the reaction mixture was poured into 800 mL of 2N HCl. The precipitate formed was collected by filtration, co-evaporated twice with toluene and dried under high vacuum at 55° C. 1H NMR (400 MHz, acetone-d6): 11.1 (bs, 1H), 7.76 (d, 1H), 7.18 (d, 1H), 7.14 (s, 1H), 5.60 (s, 1H), 2.47 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07960409B2 |
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| Quelldatensatz | uspto-grants-2011_06 |
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| ORD ID | ord-51e75555139f4c4e9129d87f44530ea9 |
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| Quellennotiz | uspto-grants-2011_06 |
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