HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576065Generated: October 31, 2026
Dichloromaleic anhydride → 3-(2',3'-Dichloromaleinimidyl)-phthalic anhydride
https://huagongshe.com/reaction/1576065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromaleic anhydride | HCID 70728 | — |
| Reactant | 3-Aminophthalic acid | HCID 79490 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(2',3'-Dichloromaleinimidyl)-phthalic anhydride | HCID 54427493 | 58% |
Reaction Steps
20 g (0.12 mol) of 2,3-dichloromaleic anhydride are added to a solution of 18.1 g (0.1 mol) of 3-aminophthalic acid in 90 ml of dioxane. The reaction mixture is stirred at 20°-30°C, whereupon a clear solution is produced over the course of approx. 30 minutes. The dioxane is then distilled off in vacuo (20 mm Hg) and the oil which remains is warmed to 130°C. After 3 hours, the crystalline mass is cooled to 50°C and mixed with 100 ml of ethyl acetate. The reaction product is filtered off at 10°C and dried in vacuo at 80°C. 18.1 g (58% of theory) of crystalline 3-(2',3'-dichloromaleinimidyl)-phthalic anhydride are obtained, melting at 229°-230°C after recyrstallisation from anhydrous acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03979393 |
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| Source dataset | uspto-grants-1976_09 |
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| ORD ID | ord-8d7bc36eb85f4b0d83e922a38d650984 |
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| Source note | uspto-grants-1976_09 |
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