Ethanol → 4-Chloro-2-(propan-2-yl)pent-4-enoic acid
反応式
[Cl:1][C:2](=[CH2:13])[CH2:3][CH:4]([CH:10]([CH3:12])[CH3:11])[C:5]([O:7]CC)=[O:6].C(O)C.[OH-].[Na+]>O>[Cl:1][C:2](=[CH2:13])[CH2:3][CH:4]([CH:10]([CH3:11])[CH3:12])[C:5]([OH:7])=[O:6]参加物
5
実験手順
The ethyl 4-chloro-2-isopropyl-4-pentenoate (8.0 g, 0.039 mol) was refluxed for 20 hrs. in 15 ml of water and 15 ml of ethanol containing 4.8 g (0.12 mol) of sodium hydroxide. Most of the ethanol was removed on the rotary evaporator and the residue taken up in 100 ml of water. The aqueous solution was extracted with two 50 ml portions of ether, then acidified with conc. HCl. The acidified mixture was extracted twice with 100 ml of ether. The ether was washed with water, dried (MgSO4), and removed to leave 4.83 g (70% yield) of a light yellow oil.
後処理
- customMost of the ethanol was removed on the rotary evaporator
- extractionThe aqueous solution was extracted with two 50 ml portions of ether
- extractionThe acidified mixture was extracted twice with 100 ml of ether
- washThe ether was washed with water
- dry with materialdried (MgSO4)
- customremoved
出典と根拠
- ORDレコード
- ord-f9a2d4deca2843888358603d67f89cf2
- 出典データセット
- uspto-grants-1985_01
- 特許番号
- US04492799
反応ノート
読み込み中…