Acetaldehyde → Methyl 2-bromomethyl-2-butenoate
反応式
[C:1]([O:5][CH3:6])(=[O:4])[CH:2]=[CH2:3].[CH:7](=O)[CH3:8].S(=O)(=O)(O)O.[BrH:15]>>[Br:15][CH2:3][C:2](=[CH:7][CH3:8])[C:1]([O:5][CH3:6])=[O:4]参加物
5
実験手順
In a manner to that of S. E. Drews, D. Emsley, et al., in J. Chem. Soc., Perkin Transaction I, pp. 2079 and 2079 (1982), an ice cooled solution of methyl acrylate (IV) (8.6 g) in conc. HBr (16.5 ml) is mixed dropwise with acetaldehyde (V) (4.4 g) and then conc. sulfuric acid (15 ml). After stirring overnight, the reaction mixture is extracted thrice with ether. The extract is washed with saturated saline, dried over MgSO4, and concentrated. The resulting residue is distilled under reduced pressure to give methyl 2-bromomethyl-2-butenoate (III) (8.59 g). 83°~85° C./10 mmHg.
後処理
- extractionthe reaction mixture is extracted thrice with ether
- washThe extract is washed with saturated saline
- dry with materialdried over MgSO4
- concentrationconcentrated
- distillationThe resulting residue is distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-a4522165b2504ffd89b9ad41a58b80ee
- 出典データセット
- uspto-grants-1990_10
- 特許番号
- US04960879
反応ノート
読み込み中…