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 | Benzene | HCID 241 | — |
| Produkt | 4-Hydroxy-7-methylcoumarin | HCID 54685307 | 79% |
Reaktionsschritte
A solution of 42 g (0.28 mol) of 2-hydroxy-4-methylacetophenone in benzene (150 mL) was added over 30 min. to a suspension of NaH (50% oil), 30 g, 0.63 mol) in 400 mL of benzene at reflux. Then, diethylcarbonate (67.8 mL, 0.56 mol) in benzene (500 mL) was added over 15 min.. The reaction mixture was refluxed for 16 h and more NaH (13 g, 0.28 mol) was added followed by more diethylcarbonate (33 g, 0.28 mol). After another 6 h at reflux the reaction mixture was cooled to r.t. and HCl (2N) was added (1.5 L) to form a white precipitate. The solid was then filtered and added to a solution of NaOH (4N) (800 mL). The resulting basic solution was then extracted with ET2O (2×500 mL) and the basic solution acidified with HCl conc. to give a white solid which after filtration and dried gave 38.7 g (79%) of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05552437 |
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| Quelldatensatz | uspto-grants-1996_09 |
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| ORD ID | ord-2200cc2031b6424ead2d47ac40795bba |
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| Quellennotiz | uspto-grants-1996_09 |
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