HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015445Generated: October 31, 2026
m-Chloroperbenzoic acid → HCID 67300489, compound
https://huagongshe.com/reaction/1015445
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | HCID 67300467 | HCID 67300467 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 67300489 | HCID 67300489 | — |
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 483 mg of 3-chloroperbenzoic acid under ice-cooling was added, followed by stirring at the same temperature for 30 minutes and then at room temperature for 1 hour. A 10% sodium hydrogen sulfite aqueous solution was added to the reaction liquid, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium bicarbonate aqueous solution and 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 (ethyl acetate:hexane:chloroform=0.2:1:1 to 0.3:1:1 to 0.4:1:1) to obtain 285 mg of ethyl 1-(4-fluorobenzyl)-2-methyl-3-(methylsulfonyl)-1H-indole-5-carboxylate as a pale green 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-6deb0f24e8264d1cb21c3d1338e657ce |
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| Source note | uspto-grants-2011_07 |
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