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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371138Generated: October 25, 2026

N-Ethylmaleimide → 3-(3,4-dichlorophenyl)-1-ethyl-1H-pyrrole-2,5-dione

https://huagongshe.com/reaction/371138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-EthylmaleimideHCID 4362—
Reactant3,4-DichloroanilineHCID 7257—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
SolventAcetoneHCID 180—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product3-(3,4-dichlorophenyl)-1-ethyl-1H-pyrrole-2,5-dioneHCID 13519573—

Reaction Conditions

Temperature15 °C

Reaction Steps

A 260 g portion of 3,4-dichloroaniline was dissolved in a mixture of 400 ml of concentrated hydrochloric acid and 1.5 liters of water, cooled to 15° C. in an ice-salt bath. A solution of 111 g of sodium nitrite in 250 ml of water was added dropwise, with stirring, over a 90 minute period. Then 40 g of cupric chloride dihydrate was added followed by 200 g of N-ethylmaleimide in one liter of warm acetone. The reaction mixture was cooled to 10° C. and sodium bicarbonate was added in portions over 2 hours to adjust the pH to 3.5. The mixture was allowed to stand for 48 hours. The precipitate formed was collected, air dried, and taken up in 2.5 liters of isopropanol, then 185 ml of 2,6-lutidine was added and the mixture was heated to boiling, then poured into water and allowed to stand. The solid was collected and dried. Recrystallization from acetone gave 187.1 g of 3-(3,4-dichlorophenyl)-1-ethyl-1H-pyrrole-2,5-dione as a yellow solid, mp 138°-141° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529736
Source datasetuspto-grants-1985_07
ORD IDord-04dc93a0f94b4d1a950b35f664962790
Source noteuspto-grants-1985_07