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HRID 1852248Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1852248

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-tert-ButylbenzonitrileHCID 77883—
EduktN,N-diethyl-4-methoxy-2-methyl-benzamideHCID 11053218—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(4-(tert-butyl)phenyl)-6-methoxyisoquinolin-1(2H)-oneHCID 7097901851,8%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08957203B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-4c73b52e940a4ebda95a89a788bad121
Quellennotizuspto-grants-2015_02