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HRID 1270716作成日:2026年10月27日

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

https://huagongshe.com/reaction/1270716

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TriphenylphosphineHCID 11776—
反応物4-Bromo-2,3,5,6-tetrafluoroanilineHCID 618671—
反応物(3-Methoxyphenyl)boronic acidHCID 2734370—
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

2,3,5,6-Tetrafluoro-4-bromoaniline (7.5 g, 30.7 mmol) is dissolved in DME (150 mL) and treated with 3-methoxyphenylboronic acid (4.7 g, 30.7 mmol), a catalytic amount of tetrakistriphenylphosphine palladium(0) (0.70 g, 0.6 mmol) and triphenylphosphine (0.66 g, 2.5 mmol). Potassium carbonate (8.5 μg in 50 mL of water) is added and the reaction mixture stirred and 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-c0a8c1fe4a3c4fe9b0f239282dd887b2
出典メモuspto-grants-2007_04