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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118791Generated: November 1, 2026

Potassium Hydroxide → 2-[3-(4-Acetyl-3-hydroxy-2-propylphenoxy)propylthio]benzimidazole

https://huagongshe.com/reaction/2118791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1-[4-(3-bromopropoxy)-2-hydroxy-3-propylphenyl]ethanoneHCID 2775221—
ReactantHCID 178527775HCID 178527775—
SolventEthanolHCID 702—
SolventWater methylene chlorideHCID 21908982—
Product2-[3-(4-Acetyl-3-hydroxy-2-propylphenoxy)propylthio]benzimidazoleHCID 1377146381.4%

Reaction Steps

To a suspension of 1.2 g of 2-mercaptobenzimidazole in 30 ml of ethanol was added 580 mg of potassium hydroxide under stirring and stirred at room termperature for 10 minutes. To this solution was added 2.8 g of 3-(4-acetyl-3-hydroxy-2-propylphenoxy)propylbromide at one time, and stirred at room temperature for 4 hours. The solvent was distilled off under reduced pressure and resulting residue was diluted with dichloromethane-water, then extracted with dichloromethane three times. The organic layer was combined, then washed with water saturated with sodium chloride and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, the resulting residue was recrystallized from dichloromethane-n-hexane to give 2.5 g (yield 81%) of the aimed compound as colorless powder. mp 149°-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04680398
Source datasetuspto-grants-1987_07
ORD IDord-9f018023b8264c6d8d4c2228b2e7daaa
Source noteuspto-grants-1987_07