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HRID 2108181作成日:2026年10月27日

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

https://huagongshe.com/reaction/2108181

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物Maleic AnhydrideHCID 7923—
反応物Benzenamine, 3-ethynyl-HCID 104682—
触媒Nickel acetate tetrahydrateHCID 62601—
溶媒WaterHCID 962—
生成物1H-Pyrrole-2,5-dione, 1-(3-ethynylphenyl)-HCID 71006080.1%

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04937356
出典データセットuspto-grants-1990_06
ORD IDord-39949f5565fe45a3ad4bb08b81a51216
出典メモuspto-grants-1990_06