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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34473생성일: 2026년 10월 24일

Cyclohexanone → 1-[Cyano(-methoxyphenyl)methyl]cyclohexanol

https://huagongshe.com/ko/reaction/34473

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanoneHCID 7967—
반응물HexaneHCID 8058—
반응물Ammonium ChlorideHCID 25517—
반응물Benzeneacetonitrile, 4-methoxy-HCID 66031—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-[Cyano(-methoxyphenyl)methyl]cyclohexanolHCID 20129927—

반응 조건

온도-70 °C

반응 단계

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 saturaged 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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04761501
출처 데이터셋uspto-grants-1988_08
ORD IDord-44360691b11f4f07a23280f5a70d4944
출처 메모uspto-grants-1988_08