関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Methoxyphenol | HCID 9015 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Propanoic acid, 2,3-dibromo-, butyl ester | HCID 519844 | — |
| 生成物 | Butyl-a-bromoacrylate | HCID 19901948 | 72% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04414391 |
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| 出典データセット | uspto-grants-1983_11 |
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| ORD ID | ord-38dbd090df094405a002ab58ce1d4c78 |
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| 出典メモ | uspto-grants-1983_11 |
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