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HRID 2264698생성일: 2026년 10월 24일

2-Iodoaniline → 2-[4-(tert-Butyldimethylsilanyloxy)but-1-ynyl]phenylamine

https://huagongshe.com/ko/reaction/2264698

반응식

참여 물질

역할이름HCID투입량
반응물2-IodoanilineHCID 11995—
반응물(But-3-yn-1-yloxy)(tert-butyl)dimethylsilaneHCID 4304567—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매TriethylamineHCID 8471—
생성물2-[4-(tert-Butyldimethylsilanyloxy)but-1-ynyl]phenylamineHCID 57675740—

반응 단계

2-Iodoaniline (1.76 g, 8 mmol) was dissolved in triethylamine (50 mL) and placed under N2. tert-Butylbut-3-ynyloxydimethylsilane (2.58 g, 14 mmol) was added, followed by bis(triphenylphosphine)palladium(II) chloride (30 mg, 0.042 mmol) and copper(I) iodide (7 mg, 0.036 mmol), and the reaction was stirred overnight at room temperature. Triethylamine was evaporated, and the residue was diluted with ether and filtered through Celite. The filtrate was concentrated, and the residue was purified by SiO2 chromatography (5-20% ethyl acetate/hexanes) to give the desired product. The reaction was assumed to be quantitative.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07855224B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-2cbee858c1c5450d8ef1b2159c6a4acc
출처 메모uspto-grants-2010_12