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HRID 1856616作成日:2026年10月27日

Phthalic Anhydride → 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/1856616

反応式

関与物質

役割名称HCID仕込み量
反応物Phthalic AnhydrideHCID 6811—
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物3,3'-(1,1,3,3-Tetramethyldisiloxane-1,3-diyl)bispropylamineHCID 17181—
反応物5,5'-Bi-2-benzofuran-1,1',3,3'-tetroneHCID 75494—
反応物4,4'-(Isopropylidenebis(4,1-phenyleneoxy))dianilineHCID 83119—
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—

反応手順

In accordance with the procedure of Preparation Example 1, a polyimide resin solution was obtained using 288 grams (0.98 mol) of 3,3,4,4-biphenyltetracarboxylic dianhydride as a tetracarboxylic dianhydride component, 74.6 grams (0.3 mol) of 1,3-bis(3-aminopropyl)-1,1,3,3-tetramethyldisiloxane and 287.4 grams (0.7 mol) of 2,2-bis[4-(4-aminophenoxy)-phenyl]propane as diamine components, 6 grams (0.04 mol) of phthalic anhydride as a molecular weight modifier, and 2,600 grams of NMP as a solvent. The solution was poured into 5 liters of methanol whereupon a precipitate settled out. Vacuum drying yielded 615 grams of the end polyimide resin.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06143423
出典データセットuspto-grants-2000_11
ORD IDord-d28647d92e264042ac079271c44dc419
出典メモuspto-grants-2000_11