Hydrochloric Acid → 2-Hydroxy-3,4,5-trimethyl-2-cyclopenten-1-one
反応式
C[O:2][C:3]1[C:4](=[O:11])[CH:5]([CH3:10])[CH:6]([CH3:9])[C:7]=1[CH3:8].Cl>>[OH:11][C:4]1[C:3](=[O:2])[CH:7]([CH3:8])[CH:6]([CH3:9])[C:5]=1[CH3:10]参加物
3
実験手順
5.39 g (35 mmol) of 2-methoxy-3,4,5-trimethyl-2-cyclopenten-1-one are held at reflux temperature for 90 minutes with 53.9 g (10 fold amount by weight) of 5N hydrochloric acid. The reaction mixture is extracted 3 times with 50 ml of ether each time. The combined organic phases are dried over magnesium sulphate and concentrated on a rotary evaporator. The crude product is distilled at 45°-48° C./0.03 mbar and yields 3.57 g (72.9%) of 2-hydroxy-3,4,5-trimethyl-2-cyclopenten-1-one.
後処理
- extractionThe reaction mixture is extracted 3 times with 50 ml of ether each time
- dry with materialThe combined organic phases are dried over magnesium sulphate
- concentrationconcentrated on a rotary evaporator
- distillationThe crude product is distilled at 45°-48° C./0.03 mbar
出典と根拠
- ORDレコード
- ord-e9e6388bfc2141a1b5c3bb80f3bbd920
- 出典データセット
- uspto-grants-1990_01
- 特許番号
- US04892966
反応ノート
読み込み中…