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HRID 64981作成日:2026年10月25日

Cyclohexanone → (1-Hydroxycyclohexyl)(4-methoxyphenyl)acetonitrile

https://huagongshe.com/reaction/64981

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexanoneHCID 7967—
反応物HexaneHCID 8058—
反応物Ammonium ChlorideHCID 25517—
反応物Benzeneacetonitrile, 4-methoxy-HCID 66031—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物(1-Hydroxycyclohexyl)(4-methoxyphenyl)acetonitrileHCID 9899621—

反応条件

温度-70 °C

反応手順

p-Methoxyphenylacetonitrile (50 gm, 0.3 mole) was added to dry tetrahydrofuran (250 ml) and the solution cooled to -70° C. under nitrogen. n-Butyl lithium in hexane (210 ml, 0.3 mole) was added dropwise, with stirring. The temperature was maintained below -50° C. and a yellow precipitate appeared. After the addition was complete, the reaction mixture was maintained below -50° C. for 30 minutes and cyclohexanone (35 ml, 0.3 mole) was added. After a further 45 minutes below -50° C. the temperature was allowed to rise to 0° C. and a saturated ammonium chloride solution was added. The layers were separated and the aqueous layer extracted with diethyl ether. The combined organic solution was washed with brine, dried over magnesium sulphate and evaporated. The product crystallized (25.2 gm, m.p. 125°-127° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04611078
出典データセットuspto-grants-1986_09
ORD IDord-53b0532ff7824926866cd13eab492272
出典メモuspto-grants-1986_09