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Dimethylformamide → HCID 178426271、化合物

HRID 555603
ノート
印刷プレビュー

反応式

HRID 555603 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([N:9]2[C:13](=[O:14])[CH:12]=[C:11]([CH3:15])[NH:10]2)[CH:5]=[CH:6][C:7]=1[CH3:8].P(Cl)(Cl)(Cl)=O.CN(C)[CH:23]=[O:24]>>[CH3:1][C:2]1[CH:3]=[C:4]([N:9]2[C:13]([OH:14])=[C:12]([CH:23]=[O:24])[C:11]([CH3:15])=[N:10]2)[CH:5]=[CH:6][C:7]=1[CH3:8]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 117358291-(3,4-Dimethylphenyl)-3-methyl-3-pyrazolin-5-one

生成物 1

HCID 178426271HCID 178426271、化合物収率 49%

反応条件

温度
100 °C

実験手順

1.86 g (9.16 mmol) of 1-(3,4-dimethylphenyl)-3-methyl-3-pyrazolin-5-one was dissolved in 3.6 ml of dry dimethylformamide, and 1.02 ml (11.0 mmol) of phosphorus oxychloride was added gradually under cooling with ice at 20° C. or below. After the addition, the mixture was heated at 100° C. for 2 hours, cooled to room temperature and poured into 30 ml of ice-cold water. Then, the mixture was washed with 10 ml of water and 10 ml of dimethylformamide. The mixed solution was stirred for 18 hours, and the precipitated solid was collected by filtration, washed with 20 ml of water and dried to obtain 1.03 g of the desired product as a pale brown solid (yield 49%).

後処理

  1. temperatureunder cooling with ice at 20° C. or below
  2. additionAfter the addition
  3. temperaturecooled to room temperature
  4. washThen, the mixture was washed with 10 ml of water and 10 ml of dimethylformamide
  5. filtrationthe precipitated solid was collected by filtration
  6. washwashed with 20 ml of water
  7. customdried

出典と根拠

ORDレコード
ord-60c9eece1ba045199c92a071372a279b
出典データセット
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08053453B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート