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HRID 1648974作成日:2026年10月26日

4-Methoxyphenol → Butyl-a-bromoacrylate

https://huagongshe.com/reaction/1648974

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethoxyphenolHCID 9015—
反応物Potassium HydroxideHCID 14797—
反応物Propanoic acid, 2,3-dibromo-, butyl esterHCID 519844—
生成物Butyl-a-bromoacrylateHCID 1990194872%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04414391
出典データセットuspto-grants-1983_11
ORD IDord-38dbd090df094405a002ab58ce1d4c78
出典メモuspto-grants-1983_11