Water → 3H-Phenothiazin-3-one, 4-chloro-

HRID 231041

反応式

HRID 231041 の反応式
[CH:1]1[C:14]2[C:5]([S:6][C:7]3[C:12]([N:13]=2)=[CH:11][CH:10]=[CH:9][CH:8]=3)=[CH:4][C:3](=[O:15])[CH:2]=1.[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[K+].[K+].[Cl:27]Cl.O>C(O)(=O)C>[Cl:27][C:4]1[C:3](=[O:15])[CH:2]=[CH:1][C:14]2[C:5]=1[S:6][C:7]1[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=1)[N:13]=2

参加物

6

実験手順

To a stirring solution of 500 g (2.34 mol) of 3H-phenothiazin-3-one in 12.5 liters of glacial acetic acid was added 1.25 kg of potassium dichromate. The mixture was stirred at room temperature for 1/2 hour. To this resulting mixture was then added 2.34 mol of a 1M solution of chlorine in glacial acetic acid dropwise over a period of 4 hours. The progress of the reaction was monitored by tlc to ensure no excess chlorine was added. After addition of chlorine was completed the mixture was stirred at room temperature for another 1/2 hour and was then poured into 120 liters of H2O with vigorous stirring. The 4-chloro-3H-phenothiazin-3-one which precipitated was allowed to settle overnight. The majority of the aqueous solution was siphoned off and discarded and the rest was filtered. The filtered precipitate was washed thoroughly with water and then rinsed with methanol and was allowed to dry to give 504 g crude 4-chloro-3H-phenothiazin-3-one which was recrystallized from toluene. m.p.: 221° C.

後処理

  1. additionwas added
  2. stirringwas stirred at room temperature for another 1/2 hour
  3. customThe 4-chloro-3H-phenothiazin-3-one which precipitated
  4. waitto settle overnight
  5. filtrationthe rest was filtered
  6. washThe filtered precipitate was washed thoroughly with water
  7. washrinsed with methanol
  8. customto dry

出典と根拠

ORDレコード
ord-e91534cb4aa241b5be5599bf213ba2e3
出典データセット
uspto-grants-1989_07
特許番号
US04845083

関連ノート

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