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HRID 1267219作成日:2026年10月27日

Allyl bromide → Cyclohexanone, 2-(2-propen-1-yl)-

https://huagongshe.com/reaction/1267219

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物CyclohexanoneHCID 7967—
反応物Ethyl AcetateHCID 8857—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TolueneHCID 1140—
生成物Cyclohexanone, 2-(2-propen-1-yl)-HCID 7894471.6%

反応条件

温度0 °C

反応手順

EX-6a) A suspension of potassium t-butoxide (200 g, 1.78 mol) in toluene which was cooled to 0° C. in an ice bath under N2 was treated with cyclohexanone (157 g, 1.60 mol). To the reaction mixture was slowly added allyl bromide (194 g, 1.60 mol) over a 2 hour period. The reaction was warmed to room temperature over 5 hours. The reaction was then poured into EtOAc (400 mL) and washed once with 10% potassium hydrogen sulfate (250 mL). The organic solution was then washed with brine (3×200 mL), dried over magnesium sulfate, and evaporated under reduced pressure. The resulting oil was then chromatographed to yield 158.4 g (71.6%) of 2-allyl cyclohexanone as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06552052B2
出典データセットuspto-grants-2003_04
ORD IDord-5b546ca4dfc34bd8948828b7d13c1651
出典メモuspto-grants-2003_04