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HRID 9274作成日:2026年10月24日

Potassium Carbonate → 3-Ethoxy-2-(4-fluoro-phenyl)-cyclopent-2-enone

https://huagongshe.com/ja/reaction/9274

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4-Fluorophenylboronic acidHCID 285645—
反応物2-Bromo-3-ethoxycyclopent-2-enoneHCID 10726911—
触媒TriphenylphosphineHCID 11776—
触媒(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
触媒HCID 178418789HCID 178418789—
溶媒BenzeneHCID 241—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物3-Ethoxy-2-(4-fluoro-phenyl)-cyclopent-2-enoneHCID 2198613970%

反応条件

温度100 °C

反応手順

2-Bromo-3-ethoxy-cyclopent-2-enone (Intermediate NINE2) (10.5 g, 51.2 mmol) and K2CO3 (14.2 g, 102 mmol) in toluene (100 mL), benzene (100 mL) and H2O (50 mL) was treated with a solution of 4-fluorophenylboronic acid (9.31 g, 66.5) in EtOH (100 mL). Tetrakis(triphenylphosphine)palladium(0) Pd(PPh3)4 (3 g, 2.6 mmol), bis(dibenzylideneacetone)palladium(0), Pd2(dba)3 (0.47 g, 0.5 mmol) and triphenylphosphine (0.27 g, 1.0 mmol) were added and the mixture was purged with N2 for 15 m. The mixture was heated to 100° C. for 15 h. The mixture was diluted with water and EtOAc:hexane. After extracting with EtOAc:hexane, the combined organic layers were dried over MgSO4, filtered and evaporated to dryness. The crude oil was purified by column chromatography on silica gel with 2.5% EtOAc:CH2Cl2 to give 3-ethoxy-2-(4-fluoro-phenyl)-cyclopent-2-enone (Intermediate NINE3) 7.85 g (70%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091232B2
出典データセットuspto-grants-2006_08
ORD IDord-1b99ecc263fc43ae8cb7d0f030d361c9
出典メモuspto-grants-2006_08