Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731879Generated: October 26, 2026

Dimethyl Sulfoxide → 4-(p-chlorophenyl)-N-methyl phthalimide

https://huagongshe.com/reaction/1731879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant4-ChlorophenolHCID 4684—
ReactantSodium HydroxideHCID 14798—
Reactant4-Nitro-N-methylphthalimideHCID 92321—
SolventWaterHCID 962—
SolventChlorobenzeneHCID 7964—
Product4-(p-chlorophenyl)-N-methyl phthalimideHCID 2019569993.5%

Reaction Steps

In a 500 ml three-necked flask equipped with a mechanical stirrer, Dean-Stark trap/condenser, nitrogen inlet, and thermometer was added 25.71 grams (0.20 moles) of p-chlorophenol, 100 ml dimethylsulfoxide, and 150 ml of chlorobenzene. After stirring and nitrogen purging the mixture for 30 min., 15.80 grams of aqueous sodium hydroxide (50.62 wt. %; 0.20 moles) was added. The mixture was heated up to 150° C. with the azeotropic removal of the water of reaction. After the removal of water was complete the temperature was lowered to 60° C. and 41.23 grams (0.20 moles) of 4-nitro-N-methyl phthalimide was added. The mixture was stirred overnight. Upon cooling to room temperature the product precipitated from solution. Filtration, washing the precipitate with water, and recrystallization from isopropanol yielded 50.8 grams of 4-(p-chlorophenyl)-N-methyl phthalimide. The melting point was 131°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623732
Source datasetuspto-grants-1986_11
ORD IDord-2bd0b445152d4cf5a26964474a844ce0
Source noteuspto-grants-1986_11