تفاعل #1583865
ord-7c5e8be3ec6d410389410290dde758de
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىfor 3 hours
- 2ترشيحThe reaction was filtered through Celite
- 3أخرىto remove the catalyst
- 4غسيلrinsed through with ethanol (300 ml)
- 5تركيزThe filtrate was concentrated to ˜50 ml
- 6workup.ADDITIONbefore being poured
- 7درجة الحرارةinto chilled
- 8أخرىA pale orange precipitate formed which
- 9أخرىthen formed a brown oil
- 10استخلاصThe mixture was then extracted with diethyl ether
- 11غسيلthe combined organic layers washed with water (3×1 L), brine (1×500 ml)
- 12تجفيفdried over anhydrous magnesium sulphate
- 13ترشيحfiltered
- 14أخرىThe solvent was removed in vacuo
- 15أخرىto give red/brown oil
- 16أخرىThe product was recrystallised from diethyl ether (˜100 ml)
- 17أخرىto give brown solid which
- 18غسيلwas rinsed with chilled diethyl ether
الإجراء التجريبي
3-(4-hydroxyphenyl)-4-(4-methoxyphenyl)-2H-chromen-7-ol 25.5 g (70 mmoles), 10% Pd/Al2O3 3.95 g and 200 ml of ethanol were combined in a 2-neck 500 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 (300 ml). The filtrate was concentrated to ˜50 ml before being poured into chilled, stirred water (1.4 L). 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 (3×1 L), brine (1×500 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 (˜100 ml), to give brown solid which was rinsed with chilled diethyl ether to give off-white crystals 11.3 g. The 1H NMR spectrum and numbering scheme being shown below.