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HRID 606845作成日:2026年10月26日

Cesium carbonate → 3-Trifluoromethyl-5-phenylethynylpyridine

https://huagongshe.com/reaction/606845

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物PhenylacetyleneHCID 10821—
反応物3-Chloro-5-(trifluoromethyl)pyridineHCID 2736698—
触媒Bis(acetonitrile)dichloropalladiumHCID 6093782—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物3-Trifluoromethyl-5-phenylethynylpyridineHCID 6704770310%

反応手順

Charge a sealed tube under a positive pressure of argon with bis(acetonitrile)palladium (II) chloride (18 mg, 0.07 mmol), 2-dicyclohexylphosphino diphenyl (73 mg, 0.21 mmol), cesium carbonate (0.557 g, 1.71 mmol) and 3-chloro-5-trifluoromethylpyridine, (prepared essentially as described in PREPARATION 7), (0.12 g, 0.66 mmol) in acetonitrile and stir at room temperature for 25 min (Angew. Chem. Int. Ed. 42, 5993-5996, (2003)). Add phenylacetylene (0.1 mL, 0.86 mmol) and stir at 100° C. for 16 h. Cool to room temperature, dilute with water, and wash twice with ethyl acetate. Combine the ethyl acetate layers, dry (sodium sulfate), and concentrate. Purify the residue by silica gel chromatography, eluting with 100:0 to 50:50 hexanes:dichloromethane, to obtain the title compound (30 mg, 10%).

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-c56a8d459fa94d37b179bea42a95c2e4
出典メモuspto-grants-2011_03