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Dimethylformamide → Ethyl 5-chloro-4-formyl-1-isopropyl-1H-pyrazole-3-carboxylate

HRID 1862462
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HRID 1862462 반응식
[CH2:1]([O:3][C:4]([C:6]1[CH:10]=[C:9](O)[N:8]([CH:12]([CH3:14])[CH3:13])[N:7]=1)=[O:5])[CH3:2].P(Cl)(Cl)([Cl:17])=O.CN(C)[CH:22]=[O:23]>>[CH2:1]([O:3][C:4]([C:6]1[C:10]([CH:22]=[O:23])=[C:9]([Cl:17])[N:8]([CH:12]([CH3:14])[CH3:13])[N:7]=1)=[O:5])[CH3:2]
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참가 물질

4

반응물 3

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 178469364HCID 178469364, 화합물

생성물 1

HCID 58907109Ethyl 5-chloro-4-formyl-1-isopropyl-1H-pyrazole-3-carboxylate

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온도
100 °C

실험 절차

8 g of 5-hydroxy-1-isopropyl-1H-pyrazole-3-carboxylic acid ethyl ester was added portionwise to a preformed mixture of 3.44 ml of dimethylformamide and 94 ml of phosphorus oxychloride at 0° C. under nitrogen. The mixture was then heated at 100° C. for 20 h. The mixture was evaporated under reduced pressure, the residue poured into ice-cold saturated sodium hydrogen carbonate and then extracted three times with dichloromethane. The combined extracts were washed with brine then dried over anhydrous magnesium sulphate, filtered and evaporated to give 9.1 g of 5-chloro-4-formyl-1-isopropyl-1H-pyrazole-3-carboxylic acid ethyl ester as a light brown solid which was used without further purification. Mass spectrum (ESI) m/z 245 [M+H]+.

후처리

  1. customThe mixture was evaporated under reduced pressure
  2. additionthe residue poured into ice-cold saturated sodium hydrogen carbonate
  3. extractionextracted three times with dichloromethane
  4. washThe combined extracts were washed with brine
  5. dry with materialthen dried over anhydrous magnesium sulphate
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-593ba8ee9f354cbd8d5a1706e6d5263c
출처 데이터셋
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06538015B1

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