Hydrochloric Acid → 3-Acetyl-5-Ethyldihydro-2(3H)-Furanone
反応式
Cl.O1C=C[CH2:4][C:3]1=O.[C:8]([O:14][CH2:15][CH3:16])(=[O:13])[CH2:9][C:10]([CH3:12])=[O:11]>>[C:10]([CH:9]1[CH2:16][CH:15]([CH2:3][CH3:4])[O:14][C:8]1=[O:13])(=[O:11])[CH3:12]参加物
4
実験手順
The mixture was allowed to stand overnight and was transferred to a separatory funnel and acidified with 125 ml concentrated hydrochloric acid. The organic layer was separated and the water layer extracted three times with 50 ml diethyl ether. The extracts were combined with the organic layer, dried through sodium sulfate, and the diethyl ether was removed by means of a Rotovap. 182 Grams of product were obtained which when analyzed by GC indicated 83.6% lactone and 7.8% ethyl acetoacetate.
後処理
- customwas transferred to a separatory funnel
- customThe organic layer was separated
- extractionthe water layer extracted three times with 50 ml diethyl ether
- dry with materialdried through sodium sulfate
- customthe diethyl ether was removed by means of a Rotovap
- custom182 Grams of product were obtained which when
出典と根拠
- ORDレコード
- ord-1152ca29cf0443d6a45cba7eb31966cb
- 出典データセット
- uspto-grants-1993_02
- 特許番号
- US05183908
反応ノート
読み込み中…