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HRID 1852248作成日:2026年10月27日

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

https://huagongshe.com/reaction/1852248

反応式

関与物質

役割名称HCID仕込み量
反応物4-tert-ButylbenzonitrileHCID 77883—
反応物N,N-diethyl-4-methoxy-2-methyl-benzamideHCID 11053218—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-(tert-butyl)phenyl)-6-methoxyisoquinolin-1(2H)-oneHCID 7097901851.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08957203B2
出典データセットuspto-grants-2015_02
ORD IDord-4c73b52e940a4ebda95a89a788bad121
出典メモuspto-grants-2015_02