HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441199Generated: October 31, 2026
4-Aminobenzoic Acid → HCID 2341965, compound
https://huagongshe.com/reaction/1441199
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobenzoic Acid | HCID 978 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Dimethylmaleic anhydride | HCID 13010 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 2341965 | HCID 2341965 | — |
Reaction Steps
37.8 g (0.3 mol) of dimethylmaleic anhydride was slowly added to a solution of 41.1 g (0.3 mol) of p-aminobenzoic acid and 300 ml of acetone in a 250 ml flask at 10° C. The mixture was stirred for 2 hours to obtain a yellow precipitate. Thereafter, the precipitate was collected by filtration under reduced pressure and recrystallized from a solution of DMF/water (50:50 (w/w)) to give an intermediate. The intermediate was treated with sodium acetate and acetic anhydride at 85° C. for 4 hours, cooled to room temperature, and placed in an ice bath to obtain a precipitate. The precipitate was collected by filtration under reduced pressure and recrystallized from a solution of ethanol/water (50:50 (w/w)) to give N-(p-carboxyphenyl)dimethylmaleimide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07655155B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-e1876de077cb4ea28762bb59d8f524d0 |
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| Source note | uspto-grants-2010_02 |
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