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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1856616생성일: 2026년 10월 27일

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

반응식

참여 물질

역할이름HCID투입량
반응물Phthalic AnhydrideHCID 6811—
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물3,3'-(1,1,3,3-Tetramethyldisiloxane-1,3-diyl)bispropylamineHCID 17181—
반응물5,5'-Bi-2-benzofuran-1,1',3,3'-tetroneHCID 75494—
반응물4,4'-(Isopropylidenebis(4,1-phenyleneoxy))dianilineHCID 83119—
용매MethanolHCID 887—
생성물5,5'-Carbonyldi(2-benzofuran-1,3-dione)--1-(4-aminophenyl)-1,3,3-trimethyl-2,3-dihydro-1H-inden-5-amine (1/1)HCID 6454485—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06143423
출처 데이터셋uspto-grants-2000_11
ORD IDord-d28647d92e264042ac079271c44dc419
출처 메모uspto-grants-2000_11