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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Ethylmaleimide | HCID 4362 | — |
| Reactant | 3,4-Dichloroaniline | HCID 7257 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(3,4-dichlorophenyl)-1-ethyl-1H-pyrrole-2,5-dione | HCID 13519573 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04529736 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-04dc93a0f94b4d1a950b35f664962790 |
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| Source note | uspto-grants-1985_07 |
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