Реакция #4473

ord-477e144581644ea4bec3777f5ed06716

Уравнение реакции

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

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture was cooled
  2. 2
    Фильтрацияthe resulting solid filtered off
  3. 3
    Другоеdried (0.95 g)
  4. 4
    ДругоеPurification by flash chromatography (E)

Методика

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

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04725615uspto-grants-1988_02