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Dimethylformamide → HCID 178426271, 화합물

HRID 555603
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HRID 555603 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

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

생성물 1

HCID 178426271HCID 178426271, 화합물수율 49%

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온도
100 °C

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-60c9eece1ba045199c92a071372a279b
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08053453B2

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