Reaktion #1256723
ord-3d322a73b98d45699bdee5ef9869b9d5
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturthe mixture is heated
- 2Temperaturunder reflux for 3 h
- 3SonstigeAfter hydrolysis
- 4Filtrationthe deposited precipitate is filtered off with suction
- 5Waschenwashed with toluene
- 6Sonstigedried
- 7workup.DISSOLUTIONThe product is dissolved in 200 ml of acetone
- 8Temperaturthe mixture is heated
- 9Temperaturunder reflux for 5 h
- 10SonstigeThe majority of the solvent is removed under reduced pressure
- 11SonstigeThe aqueous phase is separated off
- 12Extraktionextracted with MTB ether
- 13WaschenThe combined organic phases are washed with water
- 14Trocknendried over sodium sulfate
- 15SonstigeThe solvent is removed under reduced pressure
- 16Sonstigethe crude product is recrystallised from ethanol
Vorschrift
16.6 g (78.5 mmol) of methyl 2-oxo-5-propylcyclohexanecarboxylate, 7.65 g (69.5 mmol) of resorcinol and 5.6 ml (6.1 mmol) of phosphoryl chloride are dissolved in 55 ml of toluene, and the mixture is heated under reflux for 3 h. After hydrolysis using water, the deposited precipitate is filtered off with suction, washed with toluene and dried. The product is dissolved in 200 ml of acetone, 20 g (145 mmol) of potassium carbonate and 9.00 g (57.7 mmol) of ethyl iodide are added, and the mixture is heated under reflux for 5 h. The majority of the solvent is removed under reduced pressure, and the residue is taken up in MTB ether/water. The aqueous phase is separated off and extracted with MTB ether. The combined organic phases are washed with water and dried over sodium sulfate. The solvent is removed under reduced pressure, and the crude product is recrystallised from ethanol, giving 3-ethoxy-8-propyl-7,8,9,10-tetrahydrobenzo[c]chromen-6-one as colourless crystals. The melting point is 108° C. The other physical properties are: Δ∈=−7.5 (extrapolated from 5% solution in ZLI-2857), Δn=0.1302 (5% in ZLI-4792).