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HRID 471753생성일: 2026년 10월 25일

Trimethyl-2-propynylsilane → 2-Amino-6-(3-(trimethylsilyl)prop-1-ynyl)benzonitrile

https://huagongshe.com/reaction/471753

반응식

참여 물질

역할이름HCID투입량
반응물Trimethyl-2-propynylsilaneHCID 83378—
반응물2-Amino-6-bromobenzonitrileHCID 9813038—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매TriethylamineHCID 8471—
생성물2-Amino-6-(3-(trimethylsilyl)prop-1-ynyl)benzonitrileHCID 67400216125.2%

반응 단계

To a stirred solution of trimethyl(prop-2-ynyl)silane (1.12 g, 10 mmol), 2-amino-6-bromobenzonitrile (Klaubert, D. H.; Sellstedt, J. H.; Guinosso, C. J.; Capetola, R. J.; Bell, S. C. J. Med. Chem. 1981, 24, 742) (1.0 g, 5 mmol), CuI (0.01 equiv.) in triethylamine (50 mL) was added Pd(PPh3)4 (0.1 equiv.) at room temperature under nitrogen. The reaction mixture was then refluxed under nitrogen overnight. The solvent was evaporated, and the residue was titrated with EtOAc/water. The organic layer was separated, were washed with brine, and dried over Na2SO4. After evaporation of the solvent, the residue was purified by chromatography on silica gel eluting with 15% EtOAc in hexanes to give the title compound (1.43 g, 63%) as a as a liquid. MS 229 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08633186B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-b169c76aac034637bdeed3ed70a44150
출처 메모uspto-grants-2014_01