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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13435생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/13435

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 60.1% of the target compound, 3,3′-bis(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4′-oxydianiline, 25.0% of 3-(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4′-oxydianiline, and 14.4% of the total of various imines produced by the reaction of hexafluoroacetone with the amine moiety of 4,4′-oxydianiline. 100 ml of water were added to the reaction liquid, followed by extraction with 100 ml of ethyl acetate. Then, the organic layer was washed with 50 ml of saturated sodium hydrogencarbonate aqueous solution. The organic layer was dried with magnesium sulfate, followed by filtration and distilling the solvent off, thereby obtaining 112 g of crude 3,3′-bis(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4′-oxydianiline (purity: 50.7%). This crude product was recrystallized in toluene, thereby obtaining 41.0 g of the target 3,3′-bis(1-hydroxy-1-trifluoromethyl-2,2,2-trifluoroethyl)-4,4′-oxydianiline (yield: 62%; purity: 95.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728103B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b355d3dcfb4c4195b275a07f84f0f09b
출처 메모uspto-grants-2010_06