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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 653354생성일: 2026년 10월 26일

Tetrahydrofuran → 4-(4-Formylcyclohexyl)benzonitrile

https://huagongshe.com/reaction/653354

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 purification: trans/cis ratio about 3:1, Rf-value (ethyl acetate/petroleum 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 번호US04676604
출처 데이터셋uspto-grants-1987_06
ORD IDord-eddb7b5a620f411aad9f8f9596132082
출처 메모uspto-grants-1987_06