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HRID 601457作成日:2026年10月26日

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

https://huagongshe.com/reaction/601457

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromo-2,3,5,6-tetrafluoroanilineHCID 618671—
反応物4,4,5,5-Tetramethyl-2-(4-octylphenyl)-1,3,2-dioxaborolaneHCID 58823386—
生成物2,3,5,6-Tetrafluoro-4'-octylbiphenyl-4-amineHCID 8662188991.1%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902363B2
出典データセットuspto-grants-2011_03
ORD IDord-c669efc25822460f83a51f4699a8e947
出典メモuspto-grants-2011_03