Hydrochloric Acid → 3-Phenyl-5-butyrylisoxazole

HRID 345179

反応式

HRID 345179 の反応式
[OH:1][CH:2]([C:6]1[O:10][N:9]=[C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:7]=1)[CH2:3][CH2:4][CH3:5].Cl[O-].[Na+].N1C=CC=CC=1.Cl>ClCCl>[C:2]([C:6]1[O:10][N:9]=[C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:7]=1)(=[O:1])[CH2:3][CH2:4][CH3:5]

参加物

6

反応条件

温度
20 °C

実験手順

In 12.5 ml of dichloromethane, 4.4 g (20 mmol) of 5-(1-hydroxybutyl)-3-phenylisoxazole were dissolved. While the solution was being stirred, 35.2 g (60 mmol) of a 12.7% aqueous solution of sodium hypochlorite were added dropwise to the solution. Next, a liquid mixture which had been obtained by adding 0.48 g (6.1 mmol) of pyridine to 1.0 ml of 6N hydrochloric acid) was added dropwise over 1 hour and the reaction temperature was maintained at 20° C. After completion of the reaction, the organic layer was collected and was washed successively with a 5% aqueous solution of sodium hydrogensulfite, water and 1N hydrochloric acid. The organic layer was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The residue was then recrystallized from ethanol, whereby the target compound, namely, 5-butyryl-3-phenylisoxazole was obtained as crystals.

後処理

  1. customNext, a liquid mixture which had been obtained
  2. additionwas added dropwise over 1 hour
  3. customAfter completion of the reaction
  4. customthe organic layer was collected
  5. washwas washed successively with a 5% aqueous solution of sodium hydrogensulfite, water and 1N hydrochloric acid
  6. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  7. distillationthe solvent was distilled off under reduced pressure
  8. customThe residue was then recrystallized from ethanol, whereby the target compound

出典と根拠

ORDレコード
ord-986bb4f03aa34f55917a406890616c22
出典データセット
uspto-grants-1991_10
特許番号
US05055585

関連ノート

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