HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062230Generated: October 31, 2026
Hydrogen Peroxide → 2-(2-methoxy-6-methyl-phenyl)-7-methyl-3H-quinazolin-4-one
https://huagongshe.com/reaction/2062230
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(2-cyano-5-methyl-phenyl)-2-methoxy-6-methyl-benzamide | HCID 58010932 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-methoxy-6-methyl-phenyl)-7-methyl-3H-quinazolin-4-one | HCID 136121336 | 6.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283354B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-fdd2cb17eabb4fb8b6ac865230787d4c |
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| Source note | uspto-grants-2012_10 |
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