HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207966Generated: November 1, 2026
m-Chloroperbenzoic acid → HCID 118432011, compound
https://huagongshe.com/reaction/2207966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 118431884 | HCID 118431884 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118432011 | HCID 118432011 | 45.7% |
Reaction Steps
To a mixture of 1-(3-Chloro-phenyl)-5-(4′-methylsulfanyl-biphenyl-3-yl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (127.0 mg, 0.26 mmol) prepared in Example 24 in dichloromethane (5.0 mL), was slowly added meta-chloroperbenzoic acid (77%, 69.0 mg, 0.31 mmol) at 0° C. The reaction mixture was stirred at room temperature 30 minutes, quenched with a saturated solution of sodium hydrogen carbonate, and then extracted with dichloromethane three times. The combined extract was washed with brine, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a yellow liquid residue. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/5, 1/1) to give 61.0 mg of the titled compound as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376420B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-7835be9579224245862878a6850fc1f3 |
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| Source note | uspto-grants-2016_06 |
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