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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393507Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 86753098, compound

https://huagongshe.com/reaction/2393507

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantFumaric AcidHCID 444972—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 18976095HCID 18976095—
SolventAcetoneHCID 180—
SolventChloroformHCID 6212—
ProductHCID 86753098HCID 8675309863.6%

Reaction Steps

Under ice-cooling, m-chloroperbenzoic acid (0.18 g) was gradually added in small portions to a solution of 1-[1-(dibenzothiophen-3-yl) ethyl]-1H-imidazole (0.2 g) obtained in Example 8 in chloroform (5 ml), and the mixture was stirred at the same temperature for 2 hours. A saturated sodium bicarbonate aqueous solution was added and the chloroform layer was separated and dried over anhydrous magnesium sulfate. After evaporation of the solvent, the resulting residue was purified by silica gel column chromatography to obtain an oily material from a chloroform-methanol (100:1) eluate. This oily material was dissolved in acetone and mixed with 40 mg of fumaric acid which was dissolved by heating. After cooling, the thus precipitated crystals were washed with acetone to obtain 90 mg of 3-[1-(1H-imidazo1-1-yl)ethyl]dibenzothiophene-5-oxide monofumarate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807880
Source datasetuspto-grants-1998_09
ORD IDord-97f896b473674543a61dc1ea1263c95d
Source noteuspto-grants-1998_09