تفاعل #68747
ord-6f7641894d3b4895a473f13086f5e497
معادلة التفاعل
الكواشف
لا شيء
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1استخلاصthe crude product is extracted with ethyl acetate (3×15 ml)
- 2غسيلwashed with brine (10 ml)
- 3تجفيفdried over anhydrous magnesium sulfate
- 4ترشيحfiltered
- 5أخرىthe filtrate is evaporated to dryness under reduced pressure
الإجراء التجريبي
A solution of 2-(4′-chloro-4-ethylbiphen-3-yl)-3-methoxycyclopent-2-enone (200 mg, 0.61 mmol) in acetone (4 ml) and 2M aqueous hydrochloric acid (4 ml) is heated at 120° C. for 20 minutes under microwave irradiation. The reaction mixture is diluted with water (20 ml) and 2M aqueous hydrochloric acid (10 ml), and the crude product is extracted with ethyl acetate (3×15 ml). The organic extracts are combined, washed with brine (10 ml), dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated to dryness under reduced pressure to give 2-(4′-chloro-4-ethylbiphen-3-yl)-1,3-cyclopentanedione.