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HRID 1726384作成日:2026年10月27日

Sodium Carbonate → Methyl 3-bromo-5-(4-fluorophenyl)benzoate

https://huagongshe.com/reaction/1726384

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物4-Fluorophenylboronic acidHCID 285645—
反応物Methyl 3,5-DibromobenzoateHCID 621923—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒EthanolHCID 702—
溶媒DiglymeHCID 8150—
生成物Methyl 3,5-di(4-fluorophenyl)benzoateHCID 690620424%
生成物Methyl 3-bromo-5-(4-fluorophenyl)benzoateHCID 6906841823%

反応条件

温度88 °C

反応手順

To a solution of methyl 3,5-dibromobenzoate (3.00 g, 10.2 mmol) and 4-fluoro-phenyl boronic acid (1.43 g, 10.2 mmol) in 2-methoxyethyl ether (60 ml) and ethanol (3 ml) was added Na2CO3 (saturated, 9 ml), followed by tetrakis(triphenylphosphine) palladium (0) (0.2 g). The mixture was heated at 88° C. for 1.5 h, then cooled to room temperature, partitioned between hexane and water, and the organic phase washed with brine, dried over anhydrous sodium sulfate, decanted, and the organic solution concentrated under reduced pressure. The residue was purified by silica gel chromatography (1% EtOAc in hexane) to yield methyl 3-bromo-5-(4-fluorophenyl)benzoate (intermediate XXXIVa, 0.725 g, 23%) as a white solid, and methyl 3,5-di(4-fluorophenyl)benzoate (intermediate XXXIVb, 0.128 g, 4%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07491821B2
出典データセットuspto-grants-2009_02
ORD IDord-f7d2824e37d748efbaa5e49b5eac6485
出典メモuspto-grants-2009_02