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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601457생성일: 2026년 10월 25일

4-Bromo-2,3,5,6-tetrafluoroaniline → 2,3,5,6-Tetrafluoro-4'-octylbiphenyl-4-amine

https://huagongshe.com/reaction/601457

반응식

참여 물질

역할이름HCID투입량
반응물4-Bromo-2,3,5,6-tetrafluoroanilineHCID 618671—
반응물4,4,5,5-Tetramethyl-2-(4-octylphenyl)-1,3,2-dioxaborolaneHCID 58823386—
생성물2,3,5,6-Tetrafluoro-4'-octylbiphenyl-4-amineHCID 8662188991.1%

반응 단계

A mixture of 4,4,5,5-tetramethyl-2-(4-octylphenyl)-1,3,2-dioxaborolane (415.0 mg, 1.31 mmol), 4-bromo-2,3,5,6-tetrafluorobenzenamine (213.0 mg, 0.87 mmol), and a quaternary ammonium salt (Aliquat 336, 0.090 g) was degassed three times with nitrogen before dry toluene (7.0 mL) was added. This step was followed by addition of tetrakis(triphenylphosphine) palladium (100.0 mg) and sodium carbonate (aq. 1 M, 4.0 mL), which had been deaerated for 2 hour, under nitrogen. The mixture was stirred vigorously, and heated at reflux for 20 hours. The organic phase of the resulting reaction mixture was filtered through a thin layer of Celite® and evaporated to dryness to give 0.6 g of a crude product. The crude material was purified by chromatography on silica gel (by using ethyl acetate:hexanes (1:9) as the eluent) to yield 2,3,5,6-tetrafluoro-4′-octylbiphenyl-4-amine as an off-white solid (0.280 g, 91% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902363B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-c669efc25822460f83a51f4699a8e947
출처 메모uspto-grants-2011_03