反応式
[Br:1][CH:2]([CH2:10]Br)[C:3]([O:5][CH2:6][CH2:7][CH2:8][CH3:9])=[O:4].COC1C=CC(O)=CC=1.[OH-].[K+]>>[Br:1][C:2](=[CH2:10])[C:3]([O:5][CH2:6][CH2:7][CH2:8][CH3:9])=[O:4]参加物
実験手順
n-Butyl 2,3-dibromopropionate (144 g, 0.5 mole) containing p-methoxyphenol (0.5 g) was stirred vigorously under nitrogen and at room temperature, whilst 20% w/v aqueous caustic potash solution was slowly added. The course of the dehydrobromination was constantly monitored by gas-liquid chromatography. From time to time the reaction mixture was allowed to separate and the almost neutral aqueous phase discarded, in order to maintain that effective concentration of the added base. When more than 95% of the starting material had been consumed, the reaction was stopped and the lower organic layer run off and washed with water. After drying (Na2SO4), the crude product was distilled to give a main fraction which was n-butyl 2-bromoacrylate (yield 72%), bp 92°/17 mmHg.
後処理
- additionwas slowly added
- customto separate
- temperatureto maintain that effective concentration of the added base
- customWhen more than 95% of the starting material had been consumed
- washwashed with water
- dry with materialAfter drying (Na2SO4)
- distillationthe crude product was distilled
- customto give a main fraction which
出典と根拠
- ORDレコード
- ord-38dbd090df094405a002ab58ce1d4c78
- 出典データセット
- uspto-grants-1983_11
- 特許番号
- US04414391
関連ノート
読み込み中…