HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641131Generated: October 31, 2026
m-Chloroperbenzoic acid → N2-(1,1-dimethyl-2-methylsulfinyl ethyl)-3-iodo-N1-[2-methyl-4-{2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]phthalamide
https://huagongshe.com/reaction/641131
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | N2-(1,1-dimethyl-2-methylthioethyl)-3-iodo-N1-{2-methyl-4-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl}phthalamide | HCID 10211436 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N2-(1,1-dimethyl-2-methylsulfinyl ethyl)-3-iodo-N1-[2-methyl-4-{2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]phthalamide | HCID 10211631 | 69.4% |
Reaction Steps
In 10 ml of chloroform was dissolved 0.63 g (1.0 mmol) of N2-(1,1-dimethyl-2-methylthioethyl)-3-iodo-N1-{2-methyl-4-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl}phthalamide, and the resulting solution was cooled to 0° C. To the solution was added 0.19 g (1.1 mmol) of meta-chloroperbenzoic acid. After stirring for one hour, the reaction mixture was washed with 10% aqueous solution of potassium carbonate and dried on anhydrous magnesium sulfate, and the solvent was dissolved off under reduced pressure. Thus, 0.45 g of the objective compound was obtained (yield: 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696129B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-09cc79ad106040d2a24e81c6650538aa |
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| Source note | uspto-grants-2010_04 |
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