Ethyl Acetoacetate → 3-Acetyl-5-Ethyldihydro-2(3H)-Furanone
反応式
[C:1]([O:7][CH2:8][CH3:9])(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4].O1C=C[CH2:12][C:11]1=O>>[C:3]([CH:2]1[CH2:9][CH:8]([CH2:11][CH3:12])[O:7][C:1]1=[O:6])(=[O:4])[CH3:5]参加物
3
反応条件
- 温度
- 60 °C
実験手順
The organic layer was stripped using an aspirator vacuum (60 mm) and heating the flask to 60° C. leaving a net residue of 618 g. The residue was distilled using a packed column and Perkins Triangle Head. The product obtained by distillation comprised three fractions, 164 g, 130 g, and 114 g, respectively, comprising mostly ethyl acetoacetate. The pot material was filtered and the distillation continued to obtain 16.1 g of a fourth fraction boiling below 105° C. at 5 torr that comprised 8% lactone and 887 g of a fifth fraction having a boiling point of 110-120° C. at 5 torr that comprised 92.5% of the desired product when analyzed by gas chromatography. Yield of lactone (fifth fraction) was 42%.
後処理
- customleaving a net residue of 618 g
- distillationThe residue was distilled
- customThe product obtained by distillation
- filtrationThe pot material was filtered
- distillationthe distillation
- customto obtain 16.1 g of a fourth fraction
出典と根拠
- ORDレコード
- ord-8b3151a5d9af4ac2a295554ab057b4d2
- 出典データセット
- uspto-grants-1993_02
- 特許番号
- US05183908
反応ノート
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