Dimethylformamide → Ethyl 5-chloro-4-formyl-1-isopropyl-1H-pyrazole-3-carboxylate
反応式
[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]参加物
4
反応条件
- 温度
- 100 °C
実験手順
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]+.