Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892507Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 54215893, compound

https://huagongshe.com/reaction/892507

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 19895658HCID 19895658—
SolventDichloromethaneHCID 6344—
ProductHCID 54215893HCID 5421589326.3%

Reaction Steps

101 mg of 6-acetyl-3,4-dihydro-2,2-dimethyl-4-(3-methyl-2-pyridyl)-2H-1-benzopyran were dissolved in 5 ml of dichloromethane at room temperature and 91 mg of m-chloroperbenzoic acid were added. After 1 hour the mixture was washed in succession with sodium bisulphite solution, sodium bicarbonate solution and water. The organic extract was dried over sodium sulphate and evaporated to give an oil. This oil was triturated with t-butyl methyl ether to give a solid which, after recrystallization from ethyl acetate/t-butyl methyl ether, gave 28 mg of 2-(6-acetyl-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-4-yl)-3-methylpyridine N-oxide of melting point 154°-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05118694
Source datasetuspto-grants-1992_06
ORD IDord-1519956922e2441c9bf1fc295b54b7fc
Source noteuspto-grants-1992_06