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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-[4-(3-bromopropoxy)-2-hydroxy-3-propylphenyl]ethanone | HCID 2775221 | — |
| Reactant | HCID 178527775 | HCID 178527775 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water methylene chloride | HCID 21908982 | — |
| Product | 2-[3-(4-Acetyl-3-hydroxy-2-propylphenoxy)propylthio]benzimidazole | HCID 13771463 | 81.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04680398 |
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| Source dataset | uspto-grants-1987_07 |
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| ORD ID | ord-9f018023b8264c6d8d4c2228b2e7daaa |
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| Source note | uspto-grants-1987_07 |
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