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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 110생성일: 2026년 10월 23일

Piperidine → 2-Fluoro-4-piperidin-1-ylbenzonitrile

https://huagongshe.com/ko/reaction/110

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물4-Bromo-2-fluorobenzonitrileHCID 736029—
시약Sodium t-butoxideHCID 23676156—
촉매Palladium (II) acetateHCID 4144353—
촉매2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
용매TolueneHCID 1140—
생성물2-Fluoro-4-piperidin-1-ylbenzonitrileHCID 7942184549.37%

반응 조건

온도160 °C

반응 단계

4-bromo-2-fluorobenzonitrile (119 mg, 0.59 mmol), Piperidine (0.059 mL, 0.59 mmol), Palladium(II) acetate (6.68 mg, 0.03 mmol), dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (14.18 mg, 0.03 mmol) and sodium tert-butoxide (57.2 mg, 0.59 mmol) were suspended in toluene (4 mL) and tBuOH (0.800 mL) and heated to 160°C for 10 minutes in the microwave. LCMS indicated incomplete reaction, thus, the reaction mixture was heated to 160°C for a further 20 minutes. Still incomplete reaction however, the reaction mixture was diluted with EtOAc (10 mL), and washed sequentially with water (10 mL), and saturated brine (10 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 100% EtOAc in isohexane. A yellow oil (60mg) was isolated but NMR revealed this not be the desired product. No further work done.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-2e557d69002c4320a9c5c7d56e530a90
출처 메모750 AstraZeneca ELN dataset