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HRID 373743作成日:2026年10月26日

Water → 5,5'-Carbonyldi(2-benzofuran-1,3-dione)--1-(4-aminophenyl)-1,3,3-trimethyl-2,3-dihydro-1H-inden-5-amine (1/1)

https://huagongshe.com/reaction/373743

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PyridineHCID 1049—
反応物Acetic AnhydrideHCID 7918—
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物5,5'-Bi-2-benzofuran-1,1',3,3'-tetroneHCID 75494—
溶媒MethanolHCID 887—
生成物5,5'-Carbonyldi(2-benzofuran-1,3-dione)--1-(4-aminophenyl)-1,3,3-trimethyl-2,3-dihydro-1H-inden-5-amine (1/1)HCID 6454485—

反応条件

温度60 °C

反応手順

Into a four-neck flask equipped with a thermometer, a stirrer, and a nitrogen introducing tube charged were 10.711 g (0.0364 mol) of 3,3',4,4'-biphenyltetracarboxylic dianhydride, 7.289 g (0.0364 mol) of 2,4'-diaminodiphenyl ether, and 72 g of N-methylpyrrolidone while gaseous nitrogen was passed through the flask. With stirring, reaction was allowed to proceed at room temperature for 10 hours. Due to the formation of polyamic acids having a high molecular weight, the viscosity of the reaction system increased to such a degree that stirring became difficult. After addition of a small amount of water for controlling the molecular weight, the reaction mixture was heated at 60° C. After addition of 52 g of acetic anhydride and 26 g of pyridine, the resulting mixture was allowed to stand for 12 hours at room temperature. The obtained paste was introduced into methanol, and the precipitated fine particles of a solid resin were collected. After sufficiently washed by boiling it in methanol, the solid resin was dried under a reduced pressure at 80° C. for 10 hours, to obtain a powdery polyimide resin (reduced viscosity: 0.68 dl/g) having the repeating unit represented by the following formula.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05164816
出典データセットuspto-grants-1992_11
ORD IDord-1f5a8232e227491e950fb2247c98bcbe
出典メモuspto-grants-1992_11