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HRID 271503作成日:2026年10月26日

Triphenylphosphine → 2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyridine

https://huagongshe.com/reaction/271503

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物TrimethylsilylacetyleneHCID 66111—
反応物2-Chloro-4-iodopyridineHCID 1516511—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
生成物2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyridineHCID 21985391—

反応手順

2-Chloro-4-iodo-pyridine (10.0 g, 41.8 mmol) was dissolved in 200 mL dry THF and 17.5 mL triethyl amine. This mixture was evacuated and backfilled with argon several times to remove oxygen from the solution. Triphenylphosphine (329 mg, 1.25 mmol) and bis(triphenylphosphine)palladium(II)chloride (1.47 g, 2.09 mmol) were added and the reaction mixture was stirred at room temperature for 1 h. Copper(I)iodide (239 mg, 1.25 mmol) and trimethylsilylacetylene (6.28 g, 6.39 mmol) were added. The reaction mixture was stirred at room temperature overnight. The solvent was evaporated. The residue was taken up in 500 mL water and extracted three times with ethyl acetate (500 mL each). The combined organic extracts were dried with magnesium sulfate, filtered and evaporated. The crude product was purified by chromatography on silica gel (cyclohexane/ethyl acetate 80:20). The desired product was obtained as a light brown semi solid (10 g, >100%). This material was used without any further purification for the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452909B2
出典データセットuspto-grants-2008_11
ORD IDord-1e2bfc7e92b4444bb4badf530398ff26
出典メモuspto-grants-2008_11