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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852248Generated: October 26, 2026

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

https://huagongshe.com/reaction/1852248

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzonitrileHCID 77883—
ReactantN,N-diethyl-4-methoxy-2-methyl-benzamideHCID 11053218—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-(4-(tert-butyl)phenyl)-6-methoxyisoquinolin-1(2H)-oneHCID 7097901851.8%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957203B2
Source datasetuspto-grants-2015_02
ORD IDord-4c73b52e940a4ebda95a89a788bad121
Source noteuspto-grants-2015_02