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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantN2-(1,1-dimethyl-2-methylthioethyl)-3-iodo-N1-{2-methyl-4-[2,2,2-trifluoro-1-(trifluoromethyl)ethyl]phenyl}phthalamideHCID 10211436—
SolventChloroformHCID 6212—
ProductN2-(1,1-dimethyl-2-methylsulfinyl ethyl)-3-iodo-N1-[2-methyl-4-{2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]phthalamideHCID 1021163169.4%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696129B2
Source datasetuspto-grants-2010_04
ORD IDord-09cc79ad106040d2a24e81c6650538aa
Source noteuspto-grants-2010_04