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HRID 269577作成日:2026年10月27日

Potassium Carbonate → Ethyl 4-(acetylamino)-2''-[(phenylmethyl)oxy]-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-2-carboxylate

https://huagongshe.com/reaction/269577

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Toluene ethanolHCID 21863594—
反応物2-Benzyloxy-5-trifluoromethylphenylboronic acidHCID 23005339—
反応物Ethyl 4-(acetylamino)-2'-bromo-2-biphenylcarboxylateHCID 69312172—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物Ethyl 4-(acetylamino)-2''-[(phenylmethyl)oxy]-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-2-carboxylateHCID 5873100768.7%

反応条件

温度90 °C

反応手順

A mixture of [2-[(phenylmethyl)oxy]-5-(trifluoromethyl)phenyl]boronic acid (118 mg, 0.4 mmol), ethyl 4-(acetylamino)-2′-bromo-2-biphenylcarboxylate (121 mg, 0.33 mmol), potassium carbonate (414 mg, 3 mmol) and tetrakis(triphenylphosphine)palladium(0) (39 mg, 0.033 mmol) in 1:1 toluene/ethanol (5 ml) was stirred and heated at 90° C. under nitrogen for 2 hours. After cooling the mixture was diluted with diethyl ether and water and the organic phase dried (MgSO4) and evaporated to dryness. The residue was chromatographed with ethyl acetate/iso-hexane (1:2) to yield 121 mg of the title compound as a colourless gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07446222B2
出典データセットuspto-grants-2008_11
ORD IDord-5762e637f19e499db5f736da462d0b2c
出典メモuspto-grants-2008_11