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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731719Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 20226928, compound

https://huagongshe.com/reaction/1731719

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 11275260HCID 11275260—
SolventChloroformHCID 6212—
ProductHCID 20226928HCID 2022692873.1%

Reaction Steps

To a solution of 5-methyl-3-phenylpyridazine (2.0 g) in 40 mL of CHCl3 is added m-chloroperbenzoic acid (2.9 g, 80% pure). The solution is permitted to stand at room temperature until the reaction is complete. The precipitate which forms during the reaction period is removed by filtration, and the filtrate diluted with ether. The ether solution is then washed sequentially with 10% aqueous sodium sulfite, saturated sodium bicarbonate, and saturated brine. The washed liquid is dried over MgSO4 and then concentrated in vacuo to give 1.6 g (73%) of a pale yellow crystalline solid having a melting point of 112°-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623376
Source datasetuspto-grants-1986_11
ORD IDord-7525510354dc4899bdc70b75cc832633
Source noteuspto-grants-1986_11