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Isopropanol → Propan-2-yl 4-methyl-3-oxopentanoate

HRID 2113177
ノート
印刷プレビュー

反応式

HRID 2113177 の反応式
[CH3:1][CH:2]([CH3:10])[C:3](=[O:9])[CH2:4][C:5](OC)=[O:6].C1(C)C=CC(S(O)(=O)=O)=CC=1.[CH:22]([OH:25])([CH3:24])[CH3:23]>>[CH3:1][CH:2]([CH3:10])[C:3](=[O:9])[CH2:4][C:5]([O:25][CH:22]([CH3:24])[CH3:23])=[O:6]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 3776IsopropanolHCID 6101p-Toluenesulfonic acidHCID 2759969Methyl 4-methyl-3-oxopentanoate

生成物 1

HCID 57643949Propan-2-yl 4-methyl-3-oxopentanoate収率 83%

反応条件

温度
90 °C

実験手順

Methyl 4-methyl-3-oxo-pentanoate (304 g), isopropyl alcohol (500 ml) and p-toluenesulfonic acid (3.8 g) were stirred together and heated to reflux at 90° C. After 3 hours, 400 ml of solvent was collected by distillation at atmospheric pressure. Fresh isopropyl alcohol was added and the mixture refluxed for a further 3 hours. The cycle of distillation, addition of fresh solvent and refluxing was continued until the conversion had reached 95%, determined by a peak area ratio of product: starting material of 95:5 measured by LC. The remaining volatile solvents were removed by distillation and the resultant liquid washed with 10% sodium carbonate solution and dried over anhydrous sodium sulfate and filtered to give isopropyl 4-methyl-3-oxo-pentanoate as a clear liquid (301 g, 83%).

後処理

  1. temperatureheated
  2. distillation400 ml of solvent was collected by distillation at atmospheric pressure
  3. additionFresh isopropyl alcohol was added
  4. temperaturethe mixture refluxed for a further 3 hours
  5. distillationThe cycle of distillation, addition of fresh solvent
  6. temperaturerefluxing
  7. customThe remaining volatile solvents were removed by distillation
  8. washthe resultant liquid washed with 10% sodium carbonate solution
  9. dry with materialdried over anhydrous sodium sulfate
  10. filtrationfiltered

出典と根拠

ORDレコード
ord-bf26a9e2554d43639c40002870b8d854
出典データセット
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07524955B2

反応ノート

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