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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1111498생성일: 2026년 10월 25일

Tetrahydrofuran → 4-(4-Formylcyclohexyl)benzonitrile

https://huagongshe.com/reaction/1111498

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물p-[4-(Methoxymethylene)cyclohexyl]benzonitrileHCID 19739357—
용매WaterHCID 962—
생성물4-(4-Formylcyclohexyl)benzonitrileHCID 11769829100%

반응 단계

A mixture of 4.2 g of p-[4-(methoxymethylene)cyclohexyl]benzonitrile and 100 ml of tetrahydrofuran/2N hydrochloric acid (vol. 4:1) was heated to reflux for 30 minutes in a round flask. The mixture was subsequently poured into 100 ml of water and extracted three times with 100 ml of diethyl ether each time The organic phases were washed once with 100 ml of water, dried over magnesium sulphate and concentrated There were obtained 3.9 g (100%) of 4-(p-cyanophenyl)cyclohexanecarboxaldehyde as a colourless oil which was used in the next step without further purificarion: trans/cis ratio about 3:1, Rf-value (ethyl acetate/petroleum ether, vol. 3:7) 0.41. By recrystallization from hexane there could be obtained pure trans-4 (p-cyanophenyl)cyclohexanecarboxaldehyde; m.p. 57.1° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04980486
출처 데이터셋uspto-grants-1990_12
ORD IDord-b1a963f121af4e11a3e10c9c616588d7
출처 메모uspto-grants-1990_12