反応式
[CH2:1]([CH:6]([C:12]([O:14]CC)=[O:13])[C:7]([O:9]CC)=[O:8])[CH2:2][CH:3]([CH3:5])[CH3:4]>[OH-].[Na+]>[CH2:1]([CH:6]([C:12]([OH:14])=[O:13])[C:7]([OH:9])=[O:8])[CH2:2][CH:3]([CH3:5])[CH3:4]参加物
3
実験手順
Diethyl isoamylmalonate (71.7 g) was added to a 50% aqueous solution of sodium hydroxide (60 ml), and the mixture was heated under reflux for 6 h. After cooling, the mixture was extracted with ether; the water layer was acidified with hydrochloric acid and, after saturation with sodium chloride, was extracted with ether. The extracts from the acidic aqueous layer were concentrated under reduced pressure to give isoamylmalonic acid. The obtained dicaboxylic acid was heated at 180° C. for 2 h. After distillation under reduced pressure, 5-mehyl-caproic acid was obtained. Yield: 30 g (75%), b.p. 107°-108° C./11 mmHg.
後処理
- temperaturethe mixture was heated
- temperatureunder reflux for 6 h
- temperatureAfter cooling
- extractionthe mixture was extracted with ether
- extractionafter saturation with sodium chloride, was extracted with ether
- concentrationThe extracts from the acidic aqueous layer were concentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-67c0c842e5e940739f490497b64ebaf8
- 出典データセット
- uspto-grants-1993_07
- 特許番号
- US05225439
関連ノート
読み込み中…