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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326589Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 10612690, compound

https://huagongshe.com/reaction/326589

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 10611577HCID 10611577—
SolventDichloromethaneHCID 6344—
ProductHCID 10612690HCID 1061269021.2%

Reaction Steps

m-Chloroperbenzoic acid (70% purity, 0.75 g) was added at -20° C. to a solution of 6-cyano-2,2-dimethyl-4-(2-pyridyl)-2H-1,3-benzoxazine (0.40 g) in dichloromethane (10 ml) and the mixture was stirred for 30 hours. The reaction mixture was extracted by addition of an aqueous sodium sulfite solution and ethyl acetate. The organic layer was successively washed with aqueous sodium carbonate and saturated saline solution and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was subjected to column chromatography on silica gel, and it was crystallized from isopropyl ether to obtain 2-(6-cyano-2,2-dimethyl-2H-1,3-benzoxazin-4-yl)pyridine N-oxide (0.09 g) (Compound 20). Likewise, Compounds 21 to 29, 32, 36, 38, 43, 45, 47, 49, 51, 56, 58, 60, 63, 65, 67, 69, 71, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91, 93, 95, 97, 106, 107, 108, 109, 110, 117, 118, 119 and 144 were prepared.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270308
Source datasetuspto-grants-1993_12
ORD IDord-33fea7f1b51f419ea3e95f36312a6c6a
Source noteuspto-grants-1993_12