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HRID 269567作成日:2026年10月26日

Potassium Carbonate → 2'-Bromo-5-chloro-2-[(phenylmethyl)oxy]biphenyl

https://huagongshe.com/reaction/269567

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(2-Bromophenyl)boronic acidHCID 2773294—
反応物Benzene, 4-chloro-2-iodo-1-(phenylmethoxy)-HCID 21112926—
反応物Toluene ethanolHCID 21863594—
触媒HCID 178418397HCID 178418397—
溶媒Diethylether waterHCID 21584184—
生成物2'-Bromo-5-chloro-2-[(phenylmethyl)oxy]biphenylHCID 6930941355.1%

反応手順

A mixture of 2-bromophenylboronic acid (2.01 g, 10 mmol), 4-chloro-2-iodo-1-[(phenylmethyl)oxy]benzene (3.445 g, 10 mmol), potassium carbonate (5.52 g, 40 mmol) and tetrakis(triphenylphosphine)palladium(0) (580 mg, 0.5 mmol) in 1:1 toluene/ethanol (45 ml) was stirred and heated at 90° C. under nitrogen for 2 hours when a further 1 g (4.98 mmol) of 2-bromophenylboronic acid and 0.2 g (0.17 mmol) of tetrakis(triphenylphosphine)palladium(0) were added. The mixture was heated for 6 hours then cooled, diluted with diethyl ether/water and the organic phase separated, dried (magnesium sulphate) and evaporated. The residue was purified by chromatography on silica eluting with ethyl acetate/iso-hexane (1:49) then rechromatographed eluting with dichloromethane/iso-hexane (1:9) to give 2.06 g of colourless gum which slowly crystallised.

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-dec43baa2d1b42faafbfaad440a7600e
出典メモuspto-grants-2008_11