HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653165Generated: October 26, 2026
Dimethyl Sulfoxide → 4-(p-chlorophenyl)-N-methyl phthalimide
https://huagongshe.com/reaction/653165
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 4-Chlorophenol | HCID 4684 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Nitro-N-methylphthalimide | HCID 92321 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 4-(p-chlorophenyl)-N-methyl phthalimide | HCID 20195699 | 93.5% |
Reaction Steps
In a 500 ml three-necked flash 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04675376 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-4cd71b6f536c4d7d8a15a9ec2d29df60 |
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| Source note | uspto-grants-1987_06 |
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