Réaction #429960
ord-f9f181e5f89a40b18ad706533f460adb
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1LavageThe organic phase was washed with 1M hydrochloric acid solution and brine
- 2SéchageThe organic was then dried over sodium sulfate
- 3Autrethe solvent removed
- 4Autreto give a tan solid
- 5FiltrationThis was filtered through a pad of silica gel using 20% ethylacetate in hexane
- 6workup.DISSOLUTIONThis material was then dissolved in 1,2-dichlorobenzene (150 mL)
- 7Températurerefluxed for 18 hours
- 8AutreThe solvent was removed in vacuo
- 9Autreto give a tan solid
- 10FiltrationThe mixture was then filtered through a celite pad
- 11Autrethe solvent removed in vacuo
- 12Autreto give tan solid
- 13AutreThis was chromatographed on silica gel using 20% ethyl acetate in hexane
Mode opératoire
To a solution of 4-trifluoromethyl-7-hydroxycoumarin (5.0 grams, 22.0 mmol) and potassium carbonate(3.6 grams, 26.0 mmol) in DMF (20.0 mL) at 40° C., was added 3-bromoprop-1-ene (2.0 mL, 23.0 mmol). This mixture was stirred 18 hours and then diluted with ethyl acetate. The organic phase was washed with 1M hydrochloric acid solution and brine. The organic was then dried over sodium sulfate and the solvent removed to give a tan solid. This was filtered through a pad of silica gel using 20% ethylacetate in hexane. This material was then dissolved in 1,2-dichlorobenzene (150 mL) and refluxed for 18 hours. The solvent was removed in vacuo to give a tan solid. This material was dissolved in methanol (150 mL) with 10% palladium on carbon (300.0 mg) under a hydrogen atmosphere (1 Atm) for 2 hours. The mixture was then filtered through a celite pad and the solvent removed in vacuo to give tan solid. This was chromatographed on silica gel using 20% ethyl acetate in hexane to give the titled compound.