HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816674Generated: November 1, 2026
m-Chloroperbenzoic acid → HCID 10293318, compound
https://huagongshe.com/reaction/1816674
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22493631 | HCID 22493631 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10293318 | HCID 10293318 | — |
Reaction Steps
The thus-obtained 2-[4-(4,4,4-trifluorobutoxy)pyridin-2-yl-methylthio]-1H-benzimidazole (1.27 g) was dissolved in methylene chloride (20 mL). A solution of 80% m-chloroperbenzoic acid (746 mg) in methylene chloride (10 mL) was added dropwise at −30° C., and the mixture was stirred for an hour at the same temperature. A saturated sodium bicarbonate solution (30 mL) was added to the reaction mixture. The temperature of the mixture was returned to room temperature, and the mixture was stirred for 10 minutes, followed by extraction with methylene chloride. The organic layer was washed sequentially with water and brine, and brought to dryness over sodium sulfate anhydrate. The solvent was removed under reduced pressure. The residue was subjected to silica gel column chromatography (silica gel: NH-DM1020 (product of Fuji Silicia), chloroform:methanol=10:1), whereby 2-[4-(4,4,4-trifluorobutoxy)pyridin-2-yl-methanesulfinyl]-1H-benzimidazole was obtained (1.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06884810B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-db42d1f187c34f5db8c1eab4cdcd7613 |
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| Source note | uspto-grants-2005_04 |
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