反応 #4478

ord-78fc489b6c4b4be39c7bb6d9b5564ba7

反応方程式

O=C1CCCC(=O)C1
1,3-Cyclohexanedione
Cl.NNc1ccc(OCc2ccccc2)cc1
product
Cl.NNc1ccc(OCc2ccccc2)cc1
[4-(Phenylmethoxy)phenyl]hydrazine hydrochloride
O=C1CCCc2[nH]c3ccc(OCc4ccccc4)cc3c21
title compound
収率 38.4%
O=C1CCCc2[nH]c3ccc(OCc4ccccc4)cc3c21
1,2,3,9-Tetrahydro-6-(phenylmethoxy)-4H-carbazol-4-one
収率 38.4%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度heated
  2. 2
    温度to reflux for 14 h
  3. 3
    温度to cool
  4. 4
    ろ過the precipitate filtered
  5. 5
    洗浄washed with isopropyl acetate and ether
  6. 6
    その他to give a solid
  7. 7
    その他Recrystallisation from methanol

実験手順

1,3-Cyclohexanedione (3.1 g) and the product of Stage (i) (5.6 g) in ethanol (196 ml) and water (39 ml) was stirred at room temperature for 3 h and then heated to reflux for 14 h. The resulting solution was allowed to cool, poured into water (500 ml) and the precipitate filtered and washed with isopropyl acetate and ether to give a solid. Recrystallisation from methanol gave the title compound as a solid (2.5 g) m.p. 235°-237°.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04725615uspto-grants-1988_02