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HRID 269565作成日:2026年10月27日

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

https://huagongshe.com/reaction/269565

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Ethyl 2-bromo-4-chlorobenzoateHCID 53216606—
反応物2'-Benzyloxy-biphenyl-2-boronic acidHCID 58730990—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物Ethyl 5-chloro-2''-[(phenylmethyl)oxy]-1,1':2',1''-terphenyl-2-carboxylateHCID 58731013—

反応条件

温度90 °C

反応手順

A mixture of 2′-benzyloxybiphenyl boronic acid (50 mg, 0.16 mmol), ethyl 2-bromo-4-chlorobenzoate (66 mg, 0.25 mmol), potassium carbonate (88 mg, 0.64 mmol) and tetrakis(triphenylphosphine)palladium(0) (10 mg, 5 mol %) in 1:1 toluene/ethanol (2 ml) was stirred and heated at 90° C. under nitrogen for 12 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 (1:9) to yield the title compound as a pale yellow gum. (46 mg, 66%).

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-a36b5c992b014a60a613a74fb93c144b
出典メモuspto-grants-2008_11