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HRID 1662543作成日:2026年10月26日

Isopropanol → Methyl 2'-fluoro-2-hydroxy-5'-(methyloxy)-1,1'-biphenyl-4-carboxylate

https://huagongshe.com/reaction/1662543

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物Sodium CarbonateHCID 10340—
反応物2-Fluoro-5-methoxyphenylboronic acidHCID 4157211—
反応物Methyl 3-hydroxy-4-iodobenzoateHCID 10378812—
触媒PalladiumHCID 23938—
溶媒WaterHCID 962—
生成物Methyl 2'-fluoro-2-hydroxy-5'-(methyloxy)-1,1'-biphenyl-4-carboxylateHCID 5770580777%

反応手順

To a round bottom flask containing 83.26A (1.0938 g, 3.93 mmol) and 2-fluoro-5-methoxyphenylboronic acid (0.7053 g, 4.15 mmol) (commercially available from Aldrich) was added a premixed solution of 1:1 isopropanol (6 mL) and water (6 mL). After stirring at room temperature for 5 minutes, sodium carbonate (0.5526 g, 5.21 mmol) and palladium, 10 wt % on activated carbon (0.0725 g, 0.0681 mmol) were added, and the reaction was then heated to 65° C. After 17 hours, the reaction was cooled to room temperature and then filtered through Celite. The filtrate was concentrated and then saturated aqueous ammonium chloride was added. After extracting three times with EtOAc, the organic solvent was removed under reduced pressure. The residue was purified by silica gel flash chromatography (0-40% EtOAc/hexane) to afford 83.26B (834.3 mg, 77% yield). 1H NMR (500 MHz, CDCl3) δ ppm 7.69 (2H, td, J=7.7, 1.7 Hz), 7.33 (1H, d, J=7.8 Hz), 7.14 (1H, t, J=9.0 Hz), 6.94 (1H, dt, J=9.0, 3.5 Hz), 6.89 (1H, dd, J=5.9, 3.2 Hz), 5.42 (1H, s), 3.94 (3H, s), 3.82 (3H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030354B2
出典データセットuspto-grants-2011_10
ORD IDord-a938543bd074411cbd709b6cc4893b02
出典メモuspto-grants-2011_10