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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 390272생성일: 2026년 10월 26일

Ethanol → 3-(3-Dimethoxymethyl-4-nitrophenoxy)-benzonitrile

https://huagongshe.com/reaction/390272

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Potassium CarbonateHCID 11430—
반응물3-CyanophenolHCID 13394—
반응물5-Fluoro-2-nitrobenzaldehydeHCID 587090—
생성물3-(3-Dimethoxymethyl-4-nitrophenoxy)-benzonitrileHCID 58625053—

반응 단계

A mixture of 3-cyanophenol (0.38 mol) in ethanol (600 mL) was stirred at room temperature and K2CO3 (0.29 mol) was added. 5-fluoro-2-nitrobenzaldehyde (0.18 mol) was added, and the reaction mixture was stirred and refluxed for 4 hours. The solvent was evaporated, and the residue was stirred in water and extracted with CH2Cl2. The organic layer was separated, dried, filtered off and the solvent was evaporated. The residue was triturated under diisopropyl ether, and then the formed solids were filtered off and dried to yield the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383637B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-1f2124a3aa644c6faf7e1b14e328c3a7
출처 메모uspto-grants-2013_02