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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586855Generated: November 1, 2026

Aniline → N-Phenylmaleimide

https://huagongshe.com/reaction/1586855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantMaleic AnhydrideHCID 7923—
SolventBenzeneHCID 241—
ProductN-PhenylmaleimideHCID 13662—

Reaction Conditions

Temperature10 °C

Reaction Steps

N-phenylmaleimide was synthesized in accordance with a method described in "Organic Synthesis", Vol.41, page 93. That is, 196 parts of maleic anhydride and 2,000 parts of benzene were charged into a four-necked flask. 186 parts of aniline dissolved in 200 parts of benzene were added dropwise to the resulting solution at 25° C. over one hour. The resulting product was cooled to 10° C. and crystals thus formed were filtered off and dried in vacuo to give 370 parts of a pale yellow solid substance. 316 parts of the produced pale yellow substance, 65 parts of anhydrous sodium acetate and 670 parts of acetic anhydride were charged into a flask fitted with a stirrer and a reflux cooler and heated gradually over an hour. Stirring was continued for one hour while the temperature was maintained at 100° C. The resulting product was poured into ice water to precipitate crystals. The crystals were filtered, washed with petroleum ether and dried to give 220 parts of yellow crystals. The melting point and the purity by liquid chromatography of the produced crystals were measured and found to be 88° C. and 97.5%, respectively. The produced maleimide compounds are shown in Table 1-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05216047
Source datasetuspto-grants-1993_06
ORD IDord-075b1c3620e44cec904cd743dfdea1c7
Source noteuspto-grants-1993_06