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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079315Generated: November 2, 2026

Hydrogen Peroxide → 2-(2-methoxy-6-methyl-phenyl)-7-methyl-3H-quinazolin-4-one

https://huagongshe.com/reaction/2079315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantN-(2-cyano-5-methyl-phenyl)-2-methoxy-6-methyl-benzamideHCID 58010932—
SolventEthanolHCID 702—
Product2-(2-methoxy-6-methyl-phenyl)-7-methyl-3H-quinazolin-4-oneHCID 1361213366.4%

Reaction Steps

N-(2-Cyano-5-methyl-phenyl)-2-methoxy-6-methyl-benzamide (25 g, 0.09 mol) was suspended in 500 mL EtOH, and 121.3 g of 33% aq. NaOH (1 mol, 11 equiv) was added. To this was added a 35% H2O2 solution (50 mL, 0.58 mol), and the reaction was heated to reflux. Additional H2O2 was added dropwise until the reaction mixture became clear. EtOH was removed under reduced pressure, and the precipitate formed was removed by filtration. The solution was acidified with acetic acid to pH 5, and the precipitate formed was collected by filtration. The precipitate was washed twice with water and once with diethyl ether. The product was purified over alumina using EtOAc/heptane (1:1) as an eluent. Another purification was performed, over silica gel with the same eluent to yield 2-(2-methoxy-6-methyl-phenyl)-7-methyl-3H-quinazolin-4-one (1.61 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928107B2
Source datasetuspto-grants-2011_04
ORD IDord-771d90b41de3474aad0aa772f9de6c65
Source noteuspto-grants-2011_04