Hydrochloric Acid → 3-Amino-1-(2,4-dichlorophenyl)-5-methyl-2-pyrazoline

HRID 544638

反応式

HRID 544638 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[NH:9][NH2:10].[C:11](#[N:15])/[CH:12]=[CH:13]/[CH3:14].Cl.[OH-].[Na+].[Si]([O-])([O-])([O-])[O-].[Mg+2].[Mg+2]>OCC[N+](C)(C)C.O>[NH2:15][C:11]1[CH2:12][CH:13]([CH3:14])[N:9]([C:3]2[CH:4]=[CH:5][C:6]([Cl:8])=[CH:7][C:2]=2[Cl:1])[N:10]=1

参加物

8

実験手順

A mixture of 7.8 g. of 2,4-dichlorophenylhydrazine (prepared from 2,4-dichlorohydrazine hydrochloride by treatment with 1 N sodium hydroxide), 9.9 g. of crotononitrile and 3 drops of choline (45% in methanol) is heated on a steam bath for 18 hours. The solution is mixed with 200 ml. of water then 20 ml. of concentrated hydrochloric acid is added and the mixture is refluxed for 1/2 hour, cooled and made basic with 10% sodium hydroxide to give a gummy solid. The solid is placed on a chromatography column containing 300 g. of a 200 mesh synthetic magnesium silicate adsorbent. The column is eluted with 1% acetone-hexane, 5% acetone-hexane and 10% acetone-hexane to remove most of the less polar material. The elution procedure is monitored by thin layer chromatography using the upper phase of a mixture of 2 parts benzene, one part acetone and 2 parts water; then the column is eluted with acetone to remove the crude product as a dark oil which partly crystallizes on standing. This material is chromatographed again using another 200 g. of the magnesium silicate adsorbent and eluting a colored impurity with 5% acetone-hexane. The column is then eluted with 50% acetone-hexane to collect a tan oil which solidifies on standing. The solid is recrystallized 3 times from ether-hexane to give 0.5 g. of the product of the Example as tan crystals, m.p. 109°-111° C.

後処理

  1. additionA mixture of 7.8 g
  2. additionThe solution is mixed with 200 ml
  3. temperaturethe mixture is refluxed for 1/2 hour
  4. temperaturecooled
  5. customto give a gummy solid
  6. additioncontaining 300 g
  7. washThe column is eluted with 1% acetone-hexane, 5% acetone-hexane and 10% acetone-hexane
  8. customto remove most of the less polar material
  9. washThe elution procedure
  10. additionthe upper phase of a mixture of 2 parts benzene, one part acetone and 2 parts water
  11. washthen the column is eluted with acetone
  12. customto remove the crude product as a dark oil which
  13. custompartly crystallizes
  14. customThis material is chromatographed again
  15. washof the magnesium silicate adsorbent and eluting a colored impurity with 5% acetone-hexane
  16. washThe column is then eluted with 50% acetone-hexane
  17. customto collect a tan oil which
  18. customThe solid is recrystallized 3 times from ether-hexane
  19. customto give 0.5 g

出典と根拠

ORDレコード
ord-cdb8d7245a3b4adc9a6ac4762e50abfb
出典データセット
uspto-grants-1984_05
特許番号
US04451479

関連ノート

読み込み中…