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HRID 1270717作成日:2026年10月27日

Potassium Carbonate → 2,3,5,6-Tetrafluoro-4-(3'-methoxyphenyl)aniline

https://huagongshe.com/reaction/1270717

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Tri-o-tolylphosphineHCID 80271—
反応物4-Bromo-2,3,5,6-tetrafluoroanilineHCID 618671—
反応物(3-Methoxyphenyl)boronic acidHCID 2734370—
触媒palladium(II) acetateHCID 167845—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2,3,5,6-Tetrafluoro-4-(3'-methoxyphenyl)anilineHCID 18451489—

反応条件

温度90 °C

反応手順

Alternative procedure: 2,3,5,6-Tetrafluoro-4-bromoaniline (12.0 g, 49.2 mmol) is dissolved in DME (250 mL) and treated with 3-methoxyphenylboronic acid (7.5 g, 49.2 mmol), a catalytic amount of palladium(II) acetate (0.23 g, 1.0 mmol) and tri-o-tolylphosphine (1.22 g, 4.0 mmol). Potassium carbonate (13.6 g in 50 mL water) is added and the reaction mixture stirred, purged with nitrogen, then heated to 90° C. for 24 hours. After cooling to room temperature most of the DME is removed by rotary evaporator under high vacuum. The resulting material is partitioned between EtOAc (200 mL) and water (250 mL). The organic layer is washed with brine, dried (Na2SO4) and concentrated by rotary evaporator. The crude reaction product is purified by flash chromatography (9:1 hexanes/EtOAc, then 6:4 hexanes/EtOAc) to give 2,3,5,6-tetrafluoro-4-(3′-methoxyphenyl)aniline (m.p. 94–96° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07202364B2
出典データセットuspto-grants-2007_04
ORD IDord-2811fa6bb2e04daaa00cb5e2387f1aa1
出典メモuspto-grants-2007_04