تفاعل #4473

ord-477e144581644ea4bec3777f5ed06716

معادلة التفاعل

O=C1CCCC(=NNc2ccc(Br)cc2)C1
product
O=C1CCCC(=NNc2ccc(Br)cc2)C1
1,3-Cyclohexanedione mono(4-bromophenylhydrazone)
O
water
O=C1CCCc2[nH]c3ccc(Br)cc3c21
title compound
O=C1CCCc2[nH]c3ccc(Br)cc3c21
6-Bromo-1,2,3,9-tetrahydro-4H-carbazol-4-one

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was cooled
  2. 2
    ترشيحthe resulting solid filtered off
  3. 3
    أخرىdried (0.95 g)
  4. 4
    أخرىPurification by flash chromatography (E)

الإجراء التجريبي

The product of Stage (i) (1.5 g) was heated under reflux with dry zinc chloride (16 g) in glacial acetic acid (75 ml) for 24 h. The mixture was cooled, poured into water (200 ml), and the resulting solid filtered off and dried (0.95 g). Purification by flash chromatography (E) gave the title compound as a solid (125 mg). T.l.c. (F), Rf 0.65

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04725615uspto-grants-1988_02