戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 610855作成日:2026年10月27日

4-Chlorophenyl cyclopropyl ketone → 1-[1-(p-Chlorophenyl)-2-methoxyvinyl]cyclopropane

https://huagongshe.com/reaction/610855

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chlorophenyl cyclopropyl ketoneHCID 81148—
反応物Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物1-[1-(p-Chlorophenyl)-2-methoxyvinyl]cyclopropaneHCID 5394226060%

反応条件

温度2.5 °C

反応手順

A solution of methoxymethyl triphenyl phosphonium chloride (20.5 g, 0.060 mol) in ether is cooled to -60° C., treated with a 2.5M solution of butyllithium in hexanes (25.2 mL, 0.063 mol), warmed to and stirred at 0-5° C. for 90 minutes, recooled to -60° C., treated with a solution of 4-chlorophenyl cyclopropyl ketone (9.03 g, 0.050 mol) in ether, warmed to and stirred at room temperature overnight, quenched with ethyl acetate and 2N hydrochloric acid, and extracted with ethyl acetate. The organic extracts are combined, washed sequentially with water, 2N hydrochloric acid and water, dried over anhydrous sodium sulfate, and concentrated in vacuo to obtain a residue. Flash column chromatography of the residue using silica gel and an ethyl acetate/hexanes solution (1:9) gives the title product as an oil (6.2 g, 60%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05998673
出典データセットuspto-grants-1999_12
ORD IDord-eee5c3742f254ec3b383a988b5b6bc1f
出典メモuspto-grants-1999_12