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HRID 892555作成日:2026年10月26日

4-[(2-Methylbut-3-yn-2-yl)oxy]benzonitrile → Benzyl 2-[3-(4-cyanophenoxy)-3-methyl-1-butyn-1-yl]pyridine-5-carboxylate

https://huagongshe.com/reaction/892555

反応式

関与物質

役割名称HCID仕込み量
反応物4-[(2-Methylbut-3-yn-2-yl)oxy]benzonitrileHCID 2779072—
反応物Benzyl 2-iodopyridine-5-carboxylateHCID 19895696—
触媒TriphenylphosphineHCID 11776—
触媒Palladium ChlorideHCID 24290—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒DiethylamineHCID 8021—
生成物Benzyl 2-[3-(4-cyanophenoxy)-3-methyl-1-butyn-1-yl]pyridine-5-carboxylateHCID 1989570274.9%

反応手順

12.2 g of benzyl 2-iodopyridine-5-carboxylate and 5.64 g of 4-(1,1-dimethyl-2-propynyloxy)benzonitrile were stirred with 32 mg of copper(I) iodide, 162 mg of triphenylphosphine and 180 mg of palladium(II) chloride in 280 ml of diethylamine at room temperature for 7 days under a nitrogen atmosphere. The mixture was evaporated and the residue was taken up in ethyl acetate and water. The organic phase was separated, dried over sodium sulphate and evaporated. The residue was chromatographed on silica gel using ethyl acetate/petroleum ether (1:4) for the elution. There were obtained 9.04 g of benzyl 2-[3-(4-cyanophenoxy)-3-methyl-1-butyn-1-yl]pyridine-5-carboxylate which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05118694
出典データセットuspto-grants-1992_06
ORD IDord-664c66a1d07b494b978510dba2f04462
出典メモuspto-grants-1992_06