HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354643Generated: October 26, 2026
Acetic Anhydride → N-(2-chloro-4-isopropenylphenyl)maleimide
https://huagongshe.com/reaction/354643
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-4-isopropenylaniline | HCID 20427144 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-chloro-4-isopropenylphenyl)maleimide | HCID 20427157 | 89% |
Reaction Steps
Maleic anhydride (50 g) was dissolved in 120 ml of acetone. While this solution was being kept at 15° C., 83 g of 2-chloro-4-isopropenylaniline was added thereto. The resulting reaction mixture was stirred at 15° C. for 2 hours. Then, 0.9 g of cobalt acetate tetrahydrate, 16 g of triethylamine, and 57 g of acetic anhydride were added, with stirring, to the above reaction mixture. Thereafter, the reaction mixture was heated to 60° C., stirred at that temperature for 21/2 hours, and then cooled to room temperature. After the addition of 50 ml of methyl alcohol, the reaction mixture was slowly poured into 2,000 ml of vigorously stirred water. The precipitate so formed was separated by filtration and then washed with water, with an aqueous sodium carbonate solution, and thoroughly with water. Finally, the precipitate was washed with 150 ml of methyl alcohol and then dried at 50° C. under reduced pressure to obtain 109 g of N-(2-chloro-4-isopropenylphenyl)maleimide in an 89% yield. The analytical data were as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04376206 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-5155a2d532e642d7894bcb95cd839ba2 |
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| Source note | uspto-grants-1983_03 |
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