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HRID 273401作成日:2026年10月26日

Water → Methyl 3-[4-[(4'-chloro-2'-methylbiphenyl-3-yl)methoxy]phenyl]propanoate

https://huagongshe.com/reaction/273401

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium CarbonateHCID 10340—
反応物(4-Chloro-2-methylphenyl)boronic acidHCID 5017600—
反応物Methyl 4-[(3-bromophenyl)methoxy]benzenepropanoateHCID 23136270—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 3-[4-[(4'-chloro-2'-methylbiphenyl-3-yl)methoxy]phenyl]propanoateHCID 5890315088.5%

反応条件

温度90 °C

反応手順

A mixture of methyl 3-[4-[(3-bromobenzyl)oxy]phenyl]propanoate (0.5 g, 1.43 mmol), 4-chloro-2-methylphenylboronic acid (0.30 g, 1.72 mmol), tetrakis(triphenylphosphine)palladium(0) (0.083 g, 0.072 mmol), sodium carbonate (0.46 g, 4.29 mmol), water (5 mL), ethanol (5 mL) and toluene (25 mL) was stirred under an argon atmosphere at 90° C. for 16 hrs. The reaction mixture was cooled, diluted with ethyl acetate, washed with water and saturated brine, dried and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-4/1) to give the title compound (0.50 g, yield 88%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456218B2
出典データセットuspto-grants-2008_11
ORD IDord-cbe6b4fbe9b945ec9dd0c15d5272c25b
出典メモuspto-grants-2008_11