2,4-Dimethylpyridine → 5-Bromo-2,4-dimethylpyridine

HRID 1084328ノート

反応式

HRID 1084328 の反応式
OS(O)(=O)=O.O=S(=O)=O.[CH3:10][C:11]1[CH:16]=[C:15]([CH3:17])[CH:14]=[CH:13][N:12]=1.[Br:18]Br.C([O-])([O-])=O.[Na+].[Na+]>>[Br:18][C:14]1[C:15]([CH3:17])=[CH:16][C:11]([CH3:10])=[N:12][CH:13]=1.[Br:18][C:16]1[C:11]([CH3:10])=[N:12][CH:13]=[CH:14][C:15]=1[CH3:17]

参加物

6

実験手順

150 ml of 65% strength oleum are added dropwise to 28.9 ml of 2,4-dimethylpyridine, while cooling with ice and stirring, such that the temperature does not rise above 35° C. When the solution has become homogeneous, 6.42 ml of bromine are slowly added dropwise, with stirring. The mixture is stirred at 80° C. for 31/2 hours. After cooling, it is carefully added dropwise to 1 kg of ice, neutralized with solid Na2CO3 and extracted 3 times with 300 ml of ether each time. The organic layer is separated off and dried over magnesium sulfate. After removal of the solvent by distillation in vacuo, 34.6 g of a pale yellow oil consisting of the isomers 5-bromo-2,4-dimethylpyridine and 3-bromo-2,4-dimethylpyridine are obtained. The isomers are separated by column chromatography on silicon dioxide gel to give 10 g of 5-bromo-2,4-dimethylpyridine as a colorless liquid (13.0 g of 3-bromo-2,4-dimethylpyridine).

後処理

  1. temperaturewhile cooling with ice
  2. customdoes not rise above 35° C
  3. stirringwith stirring
  4. stirringThe mixture is stirred at 80° C. for 31/2 hours
  5. temperatureAfter cooling
  6. extractionextracted 3 times with 300 ml of ether each time
  7. customThe organic layer is separated off
  8. dry with materialdried over magnesium sulfate
  9. customAfter removal of the solvent
  10. distillationby distillation in vacuo, 34.6 g of a pale yellow oil
  11. customare obtained
  12. customThe isomers are separated by column chromatography on silicon dioxide gel

出典と根拠

ORDレコード
ord-1b250b7748c64548840c6339ce197675
出典データセット
uspto-grants-1991_04
特許番号
US05004748

反応ノート

読み込み中…