HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620341Generated: October 29, 2026
Maleic Anhydride → N-(3-hydroxyphenyl)maleimide
https://huagongshe.com/reaction/620341
Participants
| Role | Name | HCID | Charge |
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| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | 3-Aminophenol | HCID 11568 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-(3-hydroxyphenyl)maleimide | HCID 5325833 | 37% |
Reaction Steps
A 54.57 gram portion of m-aminophenol (0.50 mole) and 650 milliliters of acetic acid were added to a reactor and maintained under a nitrogen atmosphere with stirring. The stirred solution was maintained at 25° C., then 49.03 grams of maleic anhydride (0.50 mole) dissolved in 100 milliliters of acetic acid was added to the reactor and heating to 110° C. commenced. The 110° C. reaction temperature was maintained for 14 hours (50,400 s), then the product was dried under vacuum by rotary evaporation at 120° C. for 30 minutes (1800 s) to a dark brown solid. The crude product was extracted with two 250 milliliter portions of o-dichlorobenzene at 120° C. The combined extracts were maintained at 2° C. for 24 hours (86,400 s) then the light yellow orange colored crystalline product was recovered by filtration and dried under vacuum at 60° C. for 24 hours (86,400 s) to provide 35.0 grams of N-(3-hydroxyphenyl) maleimide. Infrared spectrophotometric analysis of a film sample of the product confirmed the product structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04820798 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-9f160b42421e4b68b8b66c3341585ac8 |
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| Source note | uspto-grants-1989_04 |
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