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HRID 1626作成日:2026年10月25日

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

https://huagongshe.com/reaction/1626

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Bromo-5-nitrofuranHCID 233582—
反応物4-EthynylbenzonitrileHCID 4547245—
触媒HCID 178418476HCID 178418476—
溶媒AcetonitrileHCID 6342—
生成物4-[(5-Nitro-furan-2-yl)-ethynyl]benzonitrileHCID 19691951—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726195
出典データセットuspto-grants-1998_03
ORD IDord-fd2ce529eb5e4230a968d9b7a9207cfc
出典メモuspto-grants-1998_03