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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478047Generated: October 25, 2026

Acetic Anhydride → 1H-Pyrrole-2,5-dione, 1-(3-ethynylphenyl)-

https://huagongshe.com/reaction/478047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantMaleic AnhydrideHCID 7923—
ReactantBenzenamine, 3-ethynyl-HCID 104682—
CatalystNickel acetate tetrahydrateHCID 62601—
SolventWaterHCID 962—
Product1H-Pyrrole-2,5-dione, 1-(3-ethynylphenyl)-HCID 71006080.1%

Reaction Steps

Maleic anhydride (79.6 g, 0.81 mole) was added to a solution of distilled 3-aminophenylacetylene (95.1 g, 0.81 mole) dissolved in 500 mL of dry N,N'-dimethylacetamide (DMAc) at 5°-10° C. After addition, another 300 mL of DMAc was added and the mixture stirred at room temperature for two hours. Nickel acetate tetrahydrate (0.8 g) and acetic anhydride (300 mL) were added to the reaction mixture and stirring was continued for 12 hours at room temperature to affect cyclodehydration. The crude product was isolated by precipitation in water and recrystallized from methanol to provide N-(3-ethynylphenyl)maleimide (128 g, 80% yield) as a yellow crystalline solid, mp 129°-131° C. Elemental analysis calculated for C12H7NO2 : C, 73.09%; H, 3.58%; N, 7.10%. Found: C, 72.94%; H, 3.61%; N, 7.04%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04889912
Source datasetuspto-grants-1989_12
ORD IDord-c7149af7e208494380914fed1a944b35
Source noteuspto-grants-1989_12