Réaction #1135825
ord-11a6a4630b6044f995f11a0c8ff7225a
Équation de réaction
Réactifs
Conditions de réaction
Traitement
- 1Autrefor 3 hours
- 2FiltrationThe reaction was filtered through Celite
- 3Autreto remove the catalyst
- 4Lavagerinsed through with ethanol (100 ml)
- 5ConcentrationThe filtrate was concentrated to ˜15 ml
- 6workup.ADDITIONbefore being poured
- 7Températureinto chilled
- 8AutreA pale orange precipitate formed which
- 9Autrethen formed a brown oil
- 10ExtractionThe mixture was then extracted with diethyl ether
- 11Lavagethe combined organic layers washed with water (3×100 ml), brine (1×100 ml)
- 12Séchagedried over anhydrous magnesium sulphate
- 13Filtrationfiltered
- 14AutreThe solvent was removed in vacuo
- 15Autreto give red/brown oil
- 16AutreThe product was recrystallised from diethyl ether (˜15 ml)
- 17Autreto give brown solid which
- 18Lavagewas rinsed with chilled diethyl ether
- 19Autreto give off-white crystals
Mode opératoire
2.5 g of the product of step 8, 10% Pd/Al2O3 0.4 g and 50 ml of ethanol were combined in a 2-neck 100 ml round bottom flask. The reaction was hydrogenated at low pressure using standard conditions for 3 hours. The reaction was filtered through Celite to remove the catalyst, rinsed through with ethanol (100 ml). The filtrate was concentrated to ˜15 ml before being poured into chilled, stirred water (300 mL). A pale orange precipitate formed which then formed a brown oil. The mixture was then extracted with diethyl ether, the combined organic layers washed with water (3×100 ml), brine (1×100 ml), dried over anhydrous magnesium sulphate and filtered. The solvent was removed in vacuo to give red/brown oil. The product was recrystallised from diethyl ether (˜15 ml), to give brown solid which was rinsed with chilled diethyl ether to give off-white crystals. 4 crops of (IV), ˜1 g. The 1H NMR spectrum and numbering scheme being shown below.