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HRID 17097作成日:2026年10月25日

Triethylamine → 3-[(Trimethylsilyl)ethynyl]benzonitrile

https://huagongshe.com/reaction/17097

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物TrimethylsilylacetyleneHCID 66111—
反応物3-IodobenzonitrileHCID 144341—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒DichloromethaneHCID 6344—
生成物3-[(Trimethylsilyl)ethynyl]benzonitrileHCID 22570318—

反応手順

To a solution of commercially available 3-iodobenzonitrile (25 g, 0.109 mol), copper (I) iodide (2.08 g, 0.0109 mol), PdCl2(PPh3)2 (3.82 g, 0.0054 mol) and triethylamine (45.7 ml, 0.327 mol) in 250 of dry dichloromethane was added 12.8 g (0.131 mol) of trimethylsilylacetylene drop wise at 0° C. over a period of 10 min. The reaction mixture was stirred at RT over night. The reaction mixture was diluted with additional dichloromethane, filtered over Celite and the filtrate was concentrated. The crude material was purified by silica gel (60-120) column chromatography using 95:5 petrolium ether/ethyl acetate as eluent. A2.1 (20 g, 92%) was obtained as a brown solid 1H NMR, 400 MHz, CDCl3: 7.79 (s, 1H), 7.67 (d, 1H), 7.59 (d, 1H), 7.43 (t, 1H), 0.26 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737279B2
出典データセットuspto-grants-2010_06
ORD IDord-d8f6fc9db5de4087b5c620a666d81138
出典メモuspto-grants-2010_06