HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892262Generated: October 30, 2026
m-Chloroperbenzoic acid → HCID 11663363, compound
https://huagongshe.com/reaction/892262
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 11641598 | HCID 11641598 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11663363 | HCID 11663363 | 27.2% |
Reaction Steps
To a solution of 710 mg (1.46 mmol) 1-[2-(2-methyl-4-{2-[2-(E)-(4-chloro-2-fluorophenyl)-vinyl]-oxazol-4-ylmethoxy}-benzylsulfanyl)-ethyl]-1H-[1,2,3]triazole in 35 ml dichloromethane at −30° C. were added dropwise during 20 min. 493 mg (2.20 mmol) 3-chloro-perbenzoic acid (77% peracid) dissolved in 20 ml ethyl acetate. After 1 hour stirring at −30° C. the mixture was allowed to warm up over night, stirred another 48 hours at room temperature, diluted with dichloromethane, washed with sodium bicarbonate solution, then with water, dried and evaporated. Elution from silica with ethyl acetate (1–10% methanol gradient) gave as the second fraction 199 mg (27%) title compound as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005526B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-223b2c39c86c404ea7490b010264805b |
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| Source note | uspto-grants-2006_02 |
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