p-Toluenesulfonic acid → 6-cyano-3,4-dihydro-2,2-dimethyl-4-(6-oxo-1-cyclohexen-1-yl)-2H-1,4-benzoxazine

HRID 37116

反応式

HRID 37116 の反応式
[C:1]([C:3]1[CH:4]=[CH:5][C:6]2[O:11][C:10]([CH3:13])([CH3:12])[CH2:9][NH:8][C:7]=2[CH:14]=1)#[N:2].[C:15]1(=O)[CH2:20][CH2:19][CH2:18][CH2:17][C:16]1=[O:21].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[C:1]([C:3]1[CH:4]=[CH:5][C:6]2[O:11][C:10]([CH3:12])([CH3:13])[CH2:9][N:8]([C:15]3[C:16](=[O:21])[CH2:17][CH2:18][CH2:19][CH:20]=3)[C:7]=2[CH:14]=1)#[N:2]

参加物

5

実験手順

In 15 ml of toluene were dissolved 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazine, 0.33 g of cyclohexane-1,2-dione and a catalytic amount of p-toluenesulfonic acid and using a Dean-Stark trap, the solution was refluxed under heating for 4 hours. After cooling, the reaction mixture was washed with saturated aqueous sodium hydrogen carbonate solution and aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography and the resulting crude crystals were washed with ethanol to give 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-4-(6-oxo-1-cyclohexen-1-yl)-2H-1,4-benzoxazine.

後処理

  1. temperaturethe solution was refluxed
  2. temperatureunder heating for 4 hours
  3. temperatureAfter cooling
  4. washthe reaction mixture was washed with saturated aqueous sodium hydrogen carbonate solution and aqueous sodium chloride solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationthe solvent was distilled off under reduced pressure
  7. customThe residue was purified by silica gel column chromatography
  8. washthe resulting crude crystals were washed with ethanol

出典と根拠

ORDレコード
ord-543880f311e840e5a659f21d25f74264
出典データセット
uspto-grants-1995_05
特許番号
US05420126

関連ノート

読み込み中…