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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17097생성일: 2026년 10월 24일

Triethylamine → 3-[(Trimethylsilyl)ethynyl]benzonitrile

https://huagongshe.com/ko/reaction/17097

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TrimethylsilylacetyleneHCID 66111—
반응물3-IodobenzonitrileHCID 144341—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매DichloromethaneHCID 6344—
생성물3-[(Trimethylsilyl)ethynyl]benzonitrileHCID 22570318—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737279B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-d8f6fc9db5de4087b5c620a666d81138
출처 메모uspto-grants-2010_06