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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 656187생성일: 2026년 10월 23일

Potassium Carbonate → 4-(2-Methyl-5-oxo-1-cyclopenten-1-yl)benzonitrile

https://huagongshe.com/ko/reaction/656187

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물TriphenylphosphineHCID 11776—
반응물4-Cyanophenylboronic acidHCID 2734326—
반응물2-Bromo-3-methyl-2-cyclopenten-1-oneHCID 4437009—
촉매1,5-Diphenylpenta-1,4-dien-3-one;palladiumHCID 154270—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물4-(2-Methyl-5-oxo-1-cyclopenten-1-yl)benzonitrileHCID 21986159—

반응 조건

온도80 °C

반응 단계

2-Bromo-3-methyl-cyclopent-2-enone (Intermediate TEN1) (commercially available from Aldrich) (2.04 g, 11.4 mmol) and K2CO3 (3.16 g in 11 mL H2O) in toluene (45 mL) was treated with a solution 4-cyanophenylboronic acid (commercially available from Aldrich) (2.2 g, 15 mmol) in EtOH (27 mL). Tetrakis(triphenylphosphine) palladium(0) Pd(PPh3)4 (0.4 g), bis(dibenzylideneacetone) palladium(0), Pd2(dba)3 (0.055 g, ˜5 mol %) and triphenylphosphine (0.4 g) were added and the mixture was purged with N2 for 15 m. The mixture was heated to 80° 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 CH2Cl2 to give 4-(2-methyl-5-oxo-cyclopent-1-enyl)-benzonitrile (Intermediate TEN2) 1.74 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071635B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-bb988a6eaad74860aad1d0206028cbfb
출처 메모uspto-grants-2011_12