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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 519876생성일: 2026년 10월 26일

Dichloromethane → 4'-Formyl-2'-nitrobiphenyl-2-carbonitrile

https://huagongshe.com/reaction/519876

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Sodium CarbonateHCID 10340—
반응물4-Bromo-3-nitrobenzaldehydeHCID 808792—
반응물2-Cyano-phenylboric acidHCID 21708089—
촉매Tetrabutylammonium BromideHCID 74236—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매TolueneHCID 1140—
생성물4'-Formyl-2'-nitrobiphenyl-2-carbonitrileHCID 8664407447%

반응 단계

A mixture of 4-bromo-3-nitrobenzaldehyde (10.0 g), 2-cyanophenylboric acid (8.25 g), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II), dichloromethane adduct (3.45 g), tetrabutylammonium bromide (1.36 g), 2M aqueous sodium carbonate solution (40 mL) and toluene (400 mL) was refluxed under an argon atmosphere for 3 days. The reaction mixture was concentrated, and the residue was dissolved in ethyl acetate. The obtained ethyl acetate solution was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a pale-yellow solid (5.15 g, 40%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115136B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-19142a26a34e481abc610366d05741bc
출처 메모uspto-grants-2015_08