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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1852248생성일: 2026년 10월 26일

4-tert-Butylbenzonitrile → 3-(4-(tert-butyl)phenyl)-6-methoxyisoquinolin-1(2H)-one

https://huagongshe.com/reaction/1852248

반응식

참여 물질

역할이름HCID투입량
반응물4-tert-ButylbenzonitrileHCID 77883—
반응물N,N-diethyl-4-methoxy-2-methyl-benzamideHCID 11053218—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물3-(4-(tert-butyl)phenyl)-6-methoxyisoquinolin-1(2H)-oneHCID 7097901851.8%

반응 단계

To a stirred solution of N,N-diethyl-4-methoxy-2-methylbenzamide (1 g, 4.52 mmol) in THF (10 ml) was added n-BuLi (2.82 ml, 4.52 mmol, in hexane) at −78° C. and stirred for 1 h. Then to this 4-(tert-butyl)benzonitrile (0.72 g, 4.52 mmol) was added at same temperature and allowed to warm to room temperature and continued the stirring for another 1 h at room temperature. The reaction mixture was quenched with saturated NH4Cl solution and extracted with EtOac (2*100 ml). The organic phase was washed with brine, dried on Na2SO4, and evaporated under reduced pressure to get crude compound. The crude compound was purified by silica gel chromatography (20% ethyl acetate in pet ether) to get desired compound (0.72 g, 46.7%) as a solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 11.26(s, 1H), 8.11-8.09 (d, J=8 Hz, 1H), 7.73-7.71 (d, J=8 Hz, 2H), 7.52-7.50 (d, J=8 Hz, 2H), 7.06 (s, 1H), 7.05-7.03 (d, J=8 Hz, 1H), 6.82 (s, 1H), 3.89 (s, 3H), 1.32 (s, 9H); MS: MS m/z 308.2 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08957203B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-4c73b52e940a4ebda95a89a788bad121
출처 메모uspto-grants-2015_02