반응 #4473

ord-477e144581644ea4bec3777f5ed06716

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture was cooled
  2. 2
    여과the resulting solid filtered off
  3. 3
    기타dried (0.95 g)
  4. 4
    기타Purification by flash chromatography (E)

실험 절차

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

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04725615uspto-grants-1988_02