反応式
C([O:3][C:4]([CH:6]1[CH:8]([CH:9]=[C:10]([Br:12])[Br:11])[C:7]1([CH3:14])[CH3:13])=[O:5])C.[OH-].[Na+]>>[CH3:13][C:7]1([CH3:14])[CH:8]([CH:9]=[C:10]([Br:12])[Br:11])[CH:6]1[C:4]([OH:5])=[O:3]参加物
反応条件
- 温度
- 20 °C
実験手順
36.2 g. of 2,2-dimethyl-3-(2,2-dibromovinyl)-cyclopropane-1-carboxylic acid ethylester (purity: 90%, cis) trans ratio: 45:65/, 4 g. of a 25% aqueous sodium hydroxide solution and 0.2 g. of tricaprylmethyl ammonium chloride are stirred at 100° C. for 30 minutes, whereupon three 4-g. portions of the sodium hydroxide solution are added in 30 minutes intervals and stirring is continued for altogether 240 minutes. The mixture is cooled to 20° C., diluted with 100 ml. of water and extracted with 10 ml. of benzene. The aqueous solution is admixed with 12 g. of a 36% aqueous hydrochloric acid solution at 70° C. and cooled to room temperature with stirring. The precipitated acid is dissolved in 60 ml. of benzene, the solution is separated and the solvent is evaporated. 30.0 g (92%) of 2,2-dimethyl-3-(2,2-dibromovinyl)-cyclopropanecarboxylic acid are obtained. Cis/trans ratio: 40:60.
後処理
- additiondiluted with 100 ml
- extractionof water and extracted with 10 ml
- temperatureof a 36% aqueous hydrochloric acid solution at 70° C. and cooled to room temperature
- stirringwith stirring
- dissolutionThe precipitated acid is dissolved in 60 ml
- customof benzene, the solution is separated
- customthe solvent is evaporated
出典と根拠
- ORDレコード
- ord-5896fab0aaf848b38c252d58a0650131
- 出典データセット
- uspto-grants-1983_12
- 特許番号
- US04419524
関連ノート
読み込み中…