Ammonia → 3-Phenyl-6-pyridazone

HRID 238179

反応式

HRID 238179 の反応式
[C:1]1([C:7](=O)[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.O.[O:11]=[CH:12][C:13](O)=O.[NH3:16].O.[NH2:18]N>O>[C:1]1([C:7]2[CH:8]=[CH:13][C:12](=[O:11])[NH:16][N:18]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

参加物

6

反応条件

温度
40 °C

実験手順

19.6 g (162.95 mmol) of 1-phenylethanone and 5 g (54.32 mmol) of oxoacetic acid monohydrate were stirred at 100° C. for 2 hours. The reaction solution was then cooled to 40° C., and 20 ml of water and 4 ml of ammonia were added. The mixture was then extracted twice with 50 ml of dichloromethane. 2.64 ml (53.32 mmol) of hydrazine monohydrate were then added to the aqueous phase, and the mixture was stirred at 100° C. for 2 hours. After the reaction, the reaction solution was cooled to room temperature. The precipitated crystals were filtered off with suction, washed with water and dried in a vacuum drying cabinet at 50° C. overnight. This gave 4.3 g (24.97 mmol, 15% of theory) of the title compound as colorless crystals.

後処理

  1. extractionThe mixture was then extracted twice with 50 ml of dichloromethane
  2. customAfter the reaction
  3. temperaturethe reaction solution was cooled to room temperature
  4. filtrationThe precipitated crystals were filtered off with suction
  5. washwashed with water
  6. customdried in a vacuum
  7. customdrying cabinet at 50° C. overnight

出典と根拠

ORDレコード
ord-be90728811814152ae1328a5d3eae6d2
出典データセット
uspto-grants-2014_02
特許番号
US08642592B2

関連ノート

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