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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9274생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-Fluorophenylboronic acidHCID 285645—
반응물2-Bromo-3-ethoxycyclopent-2-enoneHCID 10726911—
촉매TriphenylphosphineHCID 11776—
촉매(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매HCID 178418789HCID 178418789—
용매BenzeneHCID 241—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물3-Ethoxy-2-(4-fluoro-phenyl)-cyclopent-2-enoneHCID 2198613970%

반응 조건

온도100 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091232B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-1b99ecc263fc43ae8cb7d0f030d361c9
출처 메모uspto-grants-2006_08