تفاعل #68747

ord-6f7641894d3b4895a473f13086f5e497

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصthe crude product is extracted with ethyl acetate (3×15 ml)
  2. 2
    غسيلwashed with brine (10 ml)
  3. 3
    تجفيفdried over anhydrous magnesium sulfate
  4. 4
    ترشيحfiltered
  5. 5
    أخرىthe 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08530388B2uspto-grants-2013_09