Sodium Hydroxide → 10-Nitro-7H-benzo[c]phenothiazine-8-carboxylic acid

HRID 617808ノート

反応式

HRID 617808 の反応式
[OH-].[Na+].[NH2:3][CH:4]1[CH:13]=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]1=[S:14].Cl[C:16]1[C:25]([N+:26]([O-:28])=[O:27])=[CH:24][C:23]([N+]([O-])=O)=[CH:22][C:17]=1[C:18]([O:20]C)=[O:19]>C(O)C>[N+:26]([C:25]1[CH:24]=[C:23]2[C:22](=[C:17]([C:18]([OH:20])=[O:19])[CH:16]=1)[NH:3][C:4]1[CH:13]=[CH:12][C:11]3[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=3[C:5]=1[S:14]2)([O-:28])=[O:27]

参加物

5

実験手順

5 ml of a 2 N aqueous solution of sodium hydroxide was added to a solution of 1.7 g (9.73 mmol) of 2-amino-1-naphthalenethione in ethanol (30 ml) and the obtained mixture was heated under reflux. To this mixture was added 2.54 g(9.76 mmol) of methyl 2-chloro-3,5-dinitrobenzoate and the obtained mixture was heated under reflux for 1 hour. To this mixture were added 10 ml of a 2 N aqueous solution of sodium hydroxide and 40 ml of ethanol and the obtained mixture was heated under reflux for additional 10 hours. Then it was brought back to room temperature and concentrated. After adding water, 1 N hydrochloric acid was slowly added thereto under stirring to thereby regulate the pH value to about 1. The precipitate was recovered by filtration and washed successively with ethanol and methanol to thereby give 1.14 g of the title compound.

後処理

  1. temperaturethe obtained mixture was heated
  2. temperatureunder reflux
  3. temperaturethe obtained mixture was heated
  4. temperatureunder reflux for 1 hour
  5. temperaturethe obtained mixture was heated
  6. temperatureunder reflux for additional 10 hours
  7. customwas brought back to room temperature
  8. concentrationconcentrated
  9. additionAfter adding water, 1 N hydrochloric acid
  10. additionwas slowly added
  11. filtrationThe precipitate was recovered by filtration
  12. washwashed successively with ethanol and methanol

出典と根拠

ORDレコード
ord-e02ef8d7ec0f4dc59b87f06476f89f00
出典データセット
uspto-grants-1999_09
特許番号
US05952335

反応ノート

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