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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947645Generated: October 28, 2026

2-(4-Methoxy-benzyl)-4,4-dimethyl-7-nitro-3,4-dihydro-2H-isoquinolin-1-one → 4,4-Dimethyl-7-nitro-3,4-dihydroisoquinolin-1(2H)-one

https://huagongshe.com/reaction/1947645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Methoxy-benzyl)-4,4-dimethyl-7-nitro-3,4-dihydro-2H-isoquinolin-1-oneHCID 21959362—
ReactantAmmonium cerium-nitrateHCID 57418452—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product4,4-Dimethyl-7-nitro-3,4-dihydroisoquinolin-1(2H)-oneHCID 1420995339%

Reaction Steps

A solution of 2-(4-methoxy-benzyl)-4,4-dimethyl-7-nitro-3,4-dihydro-2H-isoquinolin-1-one (1.2 g, 3.52 mmol) and cerium ammonium nitrate (5.78 g, 10.56 mmol) in acetonitrile (30 ml) and water (15 ml) was stirred at 0° C. for 1 hrs, after this time the reaction was warmed to room temperature and stirred for a further 15 h. The solvent was evaporated in vacuo and dichloromethane added. The organic phase was separated, washed with saturated aqueous ammonium chloride solution and brine, then dried and evaporated in vacuo. The crude residue was purified by flash column chromatography (15% ethyl acetate in dichloromethane) to afford the title compound (300 mg, 39%). HPLC retention time 3.71 min. Mass spectrum (ES+) m/z 221 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399481B2
Source datasetuspto-grants-2013_03
ORD IDord-14bec4d74fb849eebf588ba3d02fbf02
Source noteuspto-grants-2013_03