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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 429761생성일: 2026년 10월 26일

Hydrochloric Acid → 4-Benzyloxybenzonitrile

https://huagongshe.com/reaction/429761

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물4-CyanophenolHCID 13019—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-BenzyloxybenzonitrileHCID 56137193%

반응 단계

To a stirred solution of 4-cyanophenol (50 g, 0.42 mol) and potassium carbonate (150 g, 1.1 mol) in DMF (800 ml) was added benzyl bromide (75 ml, 0.63 mol). The reaction mixture was stirred for 2 h at room temperature before filtering off solid and reducing the filtrate in vacuo to give an oil. The solid precipitate was dissolved in water and the pH adjusted to 0.5 using 6.0M hydrochloric acid and extacted into ethyl acetate. The solvent was dried over magnesium sulphate and removed by evaporation in vacuo to give an oil. The two oil products were combined and triturated with diethyl ether/hexane to give a white solid, which was washed with hexane and dried to give the title compound (81 g, 93%). 1H NMR (CDCl3) δ 7.5 (2H, d, 1 8.6 Hz), 7.45-7.30 (5H, br m), 7.0 (2H, d, J 8.6 Hz) and 5.14 (2H, s). MS (ES) m/e 210 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06319922B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-26987c0b17784e589bc4bcd67eda28af
출처 메모uspto-grants-2001_11