Ammonia → 3-Phenyl-6-pyridazone

HRID 877220

反応式

HRID 877220 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 oxoacetate 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 twice extracted with 50 ml of dichloromethane. 2.64 ml (53.32 mmol) of hydrazine monohydrate were then added to the aqueous phase obtained, 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 twice extracted with 50 ml of dichloromethane
  2. customobtained
  3. customAfter the reaction
  4. temperaturethe reaction solution was cooled to room temperature
  5. filtrationThe precipitated crystals were filtered off with suction
  6. washwashed with water
  7. customdried in a vacuum
  8. customdrying cabinet at 50° C. overnight

出典と根拠

ORDレコード
ord-7abf0e199c0a420bbf6b4612125e53d1
出典データセット
uspto-grants-2015_03
特許番号
US08987256B2

関連ノート

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