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HRID 606928作成日:2026年10月26日

1-Fluoro-3-iodobenzene → 5-(3-Fluorophenylethynyl)-nicotinic acid ethyl ester

https://huagongshe.com/reaction/606928

反応式

関与物質

役割名称HCID仕込み量
反応物1-Fluoro-3-iodobenzeneHCID 70725—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物Ethyl 5-((trimethylsilyl)ethynyl)nicotinateHCID 67047749—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178419050HCID 178419050—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物5-(3-Fluorophenylethynyl)-nicotinic acid ethyl esterHCID 6704776280%

反応手順

Add a 1 M solution of tetrabutylammonium fluoride (0.88 g, 3.38 mmol) in tetrahydrofuran to a mixture of 3-iodofluorobenzene (0.50 g, 2.25 mmol), 5-trimethylsilanylethynyl-nicotinic acid ethyl ester, (prepared as described in PREPARATION 16), (0.84 g, 3.38 mmol), bis(triphenylphosphine)palladium (II) dichloride (0.03 g, 0.05 mmol) and copper (I) iodide (0.02 g, 0.09 mmol) at −78° C. Warm to room temperature, stir overnight and then dilute with ethyl acetate. Wash with an aqueous saturated solution of ammonium chloride, dry (magnesium sulfate), filter and concentrate. Purify the residue by silica gel chromatography, eluting with 2.5:45:52.5 ethyl acetate:chloroform:hexanes, to give the title compound as a pale yellow solid (0.46 mg, 80%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07915424B2
出典データセットuspto-grants-2011_03
ORD IDord-1237bf71b2dd440cace619e612230c93
出典メモuspto-grants-2011_03