Dimethylformamide → 4-(2-fluorophenyl)-1H-pyrazole

HRID 12437

反応式

HRID 12437 の反応式
O=P(Cl)(Cl)Cl.[F:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[CH2:13][C:14](O)=O.O.[NH2:18]N.C[N:21]([CH3:24])C=O>C(O)C>[F:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13]1[CH:14]=[N:18][NH:21][CH:24]=1

参加物

6

反応条件

温度
70 °C

実験手順

11.08 ml of N,N-dimethylformamide was slowly added dropwise to 11.03 ml of POCl3 were at 0-5° C. while stirring and, after about 5 minutes a solution of 2-fluorophenylacetic acid (6 g, 38.9 mmol) in 20 ml of N,N-dimethylformamide was added dropwise. The mixture was then heated at 70° C. for about 17 hours. The mixture was subsequently quenched with ice-water and the mixture was made alkaline by adding NaOH. The resulting solid was filtered off, the solution was extracted with dichloromethane, and the organic phase was dried and concentrated. The oil obtained in this way was directly dissolved in 50 ml of ethanol. 7.3 ml of hydrazine hydrate were added, and the reaction mixture was heated at 55° C. for 3 hours. After the reaction was complete, the solvent was evaporated and the remaining solid was stirred with water and then dried. 2.65 g of 4-(2-fluorophenyl)-1H-pyrazole were obtained.

後処理

  1. customwere at 0-5° C.
  2. additionwas added dropwise
  3. customThe mixture was subsequently quenched with ice-water
  4. additionby adding NaOH
  5. filtrationThe resulting solid was filtered off
  6. extractionthe solution was extracted with dichloromethane
  7. customthe organic phase was dried
  8. concentrationconcentrated
  9. customThe oil obtained in this way
  10. temperaturethe reaction mixture was heated at 55° C. for 3 hours
  11. customthe solvent was evaporated
  12. customdried

出典と根拠

ORDレコード
ord-0253a7c0b59e4adb8b82bec7322589c9
出典データセット
uspto-grants-2010_06
特許番号
US07728012B2

関連ノート

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