HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885814Generated: November 1, 2026
m-Chloroperbenzoic acid → HCID 14879424, compound
https://huagongshe.com/reaction/1885814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 14879254 | HCID 14879254 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 14879424 | HCID 14879424 | 68.4% |
Reaction Steps
1-(Diethylcarbamoyl)-3-(2-chloro-4-trifluoromethylphenylthio)-1,2,4-triazole (3.79 g) is dissolved in chloroform (100 ml). With the temperature held at 10° C. or below with ice water, m-chloro-perbenzoic acid (1.73 g) is added in small portions over a period of 10 minutes. Thereafter, reaction is performed at 10° C. for 2 h, then at room temperature for 10 h. The chloroform solution is washed twice with a 10% aqueous solution of potassium carbonate (100 ml), then washed with water, and dried with magnesium sulfate. When the solvent is distilled off, an oil remains. This is purified by silica gel chromatography (solvent 1:1 mixture of chloroform and n-hexane) to produce the titled compound, 1-(diethylcarbamoyl)-3-(2-chloro-4-trifluoromethylphenylsulfinyl)-1,2,4-triazole (2.7 g) as an oil; yield, 68.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05147445 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-fa741fe7e6d84c6993180d2c30a09ae7 |
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| Source note | uspto-grants-1992_09 |
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