Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622159Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 13749938, compound

https://huagongshe.com/reaction/622159

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 13654767HCID 13654767—
SolventChloroformHCID 6212—
ProductHCID 13749938HCID 1374993877.8%

Reaction Steps

To a solution of 2-[[3-methyl-4-(2,2,3,3,3-pentafluoropropoxy)-2-pyridyl]methylthio]benzimidazole (2.2 g) in chloroform (20 ml), a solution of m-chloroperbenzoic acid (*1.3 g) in chloroform (15 ml) was added dropwise while ice-cooling over a period of 30 minutes and the resulting reaction mixture was washed with a saturated aqueous sodium hydrogen carbonate. After drying over magnesium sulfate, the solvent was concentrated. The residue was applied on a silica gel (50 g) column, eluted with ethyl acetate and then recrystallized from acetone-isopropyl ether to give 1.78 g of 2-[[3-methyl-4-(2,2,3,3,3-pentafluoropropoxy)-2-pyridyl]methylsulfinyl]benzimidazole as pale yellow prisms. Melting point: 161°~163° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04769456
Source datasetuspto-grants-1988_09
ORD IDord-7da9c7799c8040018d4d377cfd766044
Source noteuspto-grants-1988_09