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HRID 128814생성일: 2026년 10월 27일

6-Chloro-3-pyridinecarbonitrile → 6-(Octyloxy)pyridine-3-carbonitrile

https://huagongshe.com/reaction/128814

반응식

참여 물질

역할이름HCID투입량
반응물6-Chloro-3-pyridinecarbonitrileHCID 5152094—
반응물Sodium octylateHCID 23689331—
용매WaterHCID 962—
생성물6-(Octyloxy)pyridine-3-carbonitrileHCID 1937515787.2%

반응 단계

A mixture of 6-chloropyridine-3-carboxamide (14 g), phosphorous oxychloride (35 ml) and chloroform (120 ml) is refluxed for 2 hr, cooled, and concentrated. The residue is stirred with water and the resulting precipitate is collected and recrystallized from ethanol to provide 10.3 g (83 %) of 6-chloropyridine-3-carbonitrile. This nitrile (2.77 g) is added to a solution of sodium octanolate (prepared from 1-octanol (2.78 g) and sodium hydride (0.88g of 60% dispersion) in DMF (20 ml)). After 30 min at room temperature, the mixture is poured into water, and the product extracted with ether. The extracts are concentrated and chromatographed with 2:3 hexane-dichloromethane, to provide 6-(octyloxy)pyridine-3-carbonitrile as a colorless oil (3.7 g, 80%). This nitrile is dissolved in toluene (15 ml), cooled to -20°, and diisobutylaluminum hydride (12.5 ml of 1.5M solution in toluene) is added dropwise. After an hour, the mixture is poured into 1.0N hydrochloric acid and the product extracted with ether. The extracts are dried, filtered, and concentrated to leave 6-(octyloxy)pyridine-3-carboxaldehyde (2.36 g) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464865
출처 데이터셋uspto-grants-1995_11
ORD IDord-25312700d82443b4a619336fff79f3f9
출처 메모uspto-grants-1995_11