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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700692Generated: October 31, 2026

m-Chloroperbenzoic acid → 7-(2-Chlorophenyl)-4-methyl-5,6,7,8-tetrahydrocinnolin-5-one-1-oxide

https://huagongshe.com/reaction/1700692

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Methyl-7-(2-chlorophenyl)-5,6,7,8-tetrahydrocinnolin-5-oneHCID 11043926—
ReactantSodium NitriteHCID 23668193—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
Product7-(2-Chlorophenyl)-4-methyl-5,6,7,8-tetrahydrocinnolin-5-one-1-oxideHCID 1831752929.3%

Reaction Steps

In benzene (10 ml) was dissolved 7-(2-chlorophenyl)-4-methyl-5,6,7,8-tetrahydrocinnolin-5-one (1.54 g), and to the solution was added m-chloroperbenzoic acid (1.72 g). The mixture was stirred at room temperature for 1 hour, and to the mixture were added ethyl acetate (300 ml), saturated sodium hydrogen carbonate solution (300 ml) and sodium nitrite (500 mg). The mixture was shaken, and the separated upper layer was washed with water and concentrated under reduced pressure. The residue was purified with silica gel column chromatography to give 7-(2-chlorophenyl)-4-methyl-5,6,7,8-tetrahydrocinnolin-5-one-1-oxide (478 mg) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-5977927d912c475d9c3a8c78819aa016
Source noteuspto-grants-2002_02