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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2091357생성일: 2026년 10월 26일

Potassium Carbonate → Cyclohexyl(5,7-difluoro-3-methyl-1-benzofuran-2-yl)methanone

https://huagongshe.com/reaction/2091357

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-(3,5-Difluoro-2-hydroxyphenyl)ethan-1-oneHCID 2736976—
반응물2-Bromo-1-cyclohexylethanoneHCID 11160027—
용매DimethylformamideHCID 6228—
생성물Cyclohexyl(5,7-difluoro-3-methyl-1-benzofuran-2-yl)methanoneHCID 6677740170%

반응 단계

To a solution (50 mL) of 1-(3,5-difluoro-2-hydroxyphenyl)ethanone (2.8 g) in N,N-dimethylformamide were added potassium carbonate (6.7 g) and 2-bromo-1-cyclohexylethanone (4.0 g) synthesized in Example A51(1) at room temperature, and the mixture was stirred at room temperature for 16 hr. The reaction mixture was allowed to cool to room temperature, and filtered through celite. Water was added to the filtrate, and the mixture was extracted with diethyl ether. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was dissolved in N,N-dimethylformamide (50 mL) again, 1,8-diazabicyclo[5.4.0]undec-7-ene (2.6 mL) was added to the solution, and the mixture was stirred at 110° C. 1 hr with heating. After cooling to room temperature, the reaction mixture was quenched with 1N hydrochloric acid, and the reaction mixture was extracted with diethyl ether. The extract was concentrated under reduced pressure, and the precipitated compound was recrystallized from diisopropyl ether-hexane to give the title object compound (3.1 g, 70%) as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08436043B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-de1b53984aef4346b5818bd559f4abc8
출처 메모uspto-grants-2013_05