HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015444Generated: October 31, 2026
m-Chloroperbenzoic acid → HCID 67300738, compound
https://huagongshe.com/reaction/1015444
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67300467 | HCID 67300467 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 67300738 | HCID 67300738 | — |
Reaction Steps
A 300 mg portion of ethyl 1-(4-fluorobenzyl)-2-methyl-3-(methylthio)-1H-indole-5-carboxylate was dissolved in 3 ml of chloroform, and 203 mg of 3-chloroperbenzoic acid was added under ice-cooling, followed by stirring at the same temperature for 1 hour. A saturated sodium bicarbonate aqueous solution was added to the reaction liquid, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and then dried over anhydrous sodium sulfate. After evaporation of the solvent under a reduced pressure, the residue was purified by silica gel column chromatography (chloroform:methanol:hexane=1:0:1 to 1:0:0 to 100:1:0 to 50:1:0 to 30:1:0) to obtain 279 mg of ethyl 1-(4-fluorobenzyl)-2-methyl-3-(methylsulfinyl)-1H-indole-5-carboxylate as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985764B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-9ede6a0996824d1ba5e4d97172b6bd60 |
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| Source note | uspto-grants-2011_07 |
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