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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6872생성일: 2026년 10월 23일

Sodium Carbonate → N-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamide

https://huagongshe.com/ko/reaction/6872

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물9-Borabicyclo(3.3.1)nonaneHCID 78966—
반응물4,4-Diethoxybut-1-eneHCID 256426—
반응물3-Bromo-N-cyclopropyl-4-fluorobenzamideHCID 22019090—
촉매HCID 178418397HCID 178418397—
용매BenzeneHCID 241—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
생성물N-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamideHCID 2201916393.4%

반응 조건

온도80 °C

반응 단계

A solution of 3-butenal diethyl acetal (144 mg, 1 mmol) and 9-BBN (0.5 M in THF, 2.2 mL, 1.1 mmol) was stirred at RT for 1 h. The mixture was concentrated and to the residue were added benzene (2 mL), EtOH (1 mL), aqueous Na2CO3 solution (2M, 1 mL), 3-bromo-4-fluoro-N-cyclopropylbenzamide (127 mg, 0.5 mmol) and Pd(Ph3P)4 (40 mg). The resulting mixture was stirred at 80° C. for 2 h. The mixture was then cooled to RT and diluted with ethyl acetate (10 mL) and washed with water. The organic layer was separated and concentrated. The residue was purified by column chromatography (SiO2; EtOAc/hexane 1:3) to afford N-cyclopropyl-3-(4,4-diethoxybutyl)-4-fluorobenzamide (151 mg, 93%). This material was dissolved in acetone (1 mL) and 3 N HCl solution (0.2 mL) and stirred at RT for 1 h. The mixture was neutralized with NaHCO3 solution and extracted with ethyl acetate (3×5 mL). The organic layer was dried and concentrated to afford N-cyclopropyl-4-fluoro-3-(4-oxo-butyl)-benzamide (110 mg, 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084160B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b66a4138f5a24ea6bea939d006b10a7b
출처 메모uspto-grants-2006_08