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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1626생성일: 2026년 10월 23일

Triethylamine → 4-[(5-Nitro-furan-2-yl)-ethynyl]benzonitrile

https://huagongshe.com/ko/reaction/1626

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Bromo-5-nitrofuranHCID 233582—
반응물4-EthynylbenzonitrileHCID 4547245—
촉매HCID 178418476HCID 178418476—
용매AcetonitrileHCID 6342—
생성물4-[(5-Nitro-furan-2-yl)-ethynyl]benzonitrileHCID 19691951—

반응 단계

To a solution of 2-bromo-5-nitrofuran (1.65 g) and triethylamine (34 ml) in anhydrous acetonitrile (55 ml) under nitrogen was added bis(triphenylphosphine)palladium dichloride (130 mg) and cuprous iodide (35 mg). 4-Ethynylbenzonitrile (1.09 g) was added and the reaction mixture was stirred under nitrogen overnight. The mixture was evaporated to dryness and the residue was dissolved in dichloromethane (200 ml), dried over anhydrous sodium sulfate, filtered and evaporated to dryness. The residue was purified by silica gel chromatography (ethyl acetate/hexane 1:10) and triturated with ethyl acetate/hexane (1:3) to give 4-[(5-nitro-2-furyl)-ethynyl]benzonitrile.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726195
출처 데이터셋uspto-grants-1998_03
ORD IDord-fd2ce529eb5e4230a968d9b7a9207cfc
출처 메모uspto-grants-1998_03