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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1853908생성일: 2026년 10월 26일

Iodoethane → 2-Ethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)butanenitrile

https://huagongshe.com/reaction/1853908

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetonitrileHCID 3842922—
용매DimethylformamideHCID 6228—
생성물2-Ethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)butanenitrileHCID 6822914738%

반응 단계

To a solution of 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetonitrile (2.0 g, 8.23 mmol) in DMF (40 mL) was cooled to 0° C. and sodium hydride (60 wt %, 1.2 g, 32.9 mmol) added portion wise. The mixture was stirred for 10 min and ethyl iodide (0.74 mL, 9.05 mmol) in THF (10 mL) was added. The mixture was stirred at room temperature for 12 h. The reaction mixture was quenched with water and diluted with ethyl acetate. The layers were separated and the organic layer was dried over anhydrous sodium sulfate, filtered, concentrated and the residue purified by column chromatography (silica, 0-30% ethyl acetate/heptane) to afford the desired product (950 mg, 38%) as a brown solid: ESI MS m/z 300 [C18H26BNO2+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08962648B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-23bd53f8e0c444068da1b35f3745bbb6
출처 메모uspto-grants-2015_02