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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13436생성일: 2026년 10월 24일

3,3'-Bis(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4'-oxydianiline → 4,4'-Diaminodiphenyl Ether

https://huagongshe.com/ko/reaction/13436

반응식

참여 물질

역할이름HCID투입량
반응물3,3'-Bis(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4'-oxydianilineHCID 86623391—
반응물3-(1-Hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4'-oxydianilineHCID 86623392—
생성물4,4'-Diaminodiphenyl EtherHCID 7579—
생성물HexafluoroacetoneHCID 12695—
생성물3,3'-Bis(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4'-oxydianilineHCID 86623391—

반응 단계

The reaction liquid was found by gas chromatography (GC) analysis to contain 59.0% of the target compound, 3,3′-bis(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4′-oxydianiline, 9.3% of 3-(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4′-oxydianiline, and 28.8% of the total of various imines produced by the reaction of hexafluoroacetone with the amine moiety of 4,4′-oxydianiline. 50 ml of toluene were added to the reaction liquid, followed by heating dissolution. After cooling, the precipitated solid matter was filtered, followed by vacuum drying. 15.2 g of crude 3,3′-bis(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4′-oxydianiline (yield: 91%; purity: 88.2%) were obtained. This crude product was recrystallized in toluene, thereby obtaining 12.0 g of the target 3,3′-bis(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4′-oxydianiline (yield: 72%; purity: 94.5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728103B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-37b33ba6a8ca458180a3763efdda179d
출처 메모uspto-grants-2010_06