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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 308생성일: 2026년 10월 24일

5-Bromo-2-methoxybenzonitrile → (R)-5-(2-(tert-butyldimethylsilyloxy)propylamino)-2-methoxybenzonitrile

https://huagongshe.com/ko/reaction/308

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참여 물질

역할이름HCID투입량
반응물5-Bromo-2-methoxybenzonitrileHCID 4418560—
반응물(R)-2-(tert-butyldimethylsilyloxy)propan-1-amineHCID 59302513—
시약Cesium carbonateHCID 10796—
촉매Palladium (II) acetateHCID 4144353—
촉매2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
용매TolueneHCID 1140—
생성물(R)-5-(2-(tert-butyldimethylsilyloxy)propylamino)-2-methoxybenzonitrileHCID 5846448862.19%

반응 조건

온도120 °C

반응 단계

Trial reaction for PdOAc2 (0.021 g, 0.09 mmol) and dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (0.045 g, 0.09 mmol) were added in one portion to a degassed solution of 5-bromo-2-methoxybenzonitrile (0.200 g, 0.94 mmol), (R)-2-(tert- butyldimethylsilyloxy)propan-1-amine (0.214 g, 1.13 mmol) and cesium carbonate (0.461 g, 1.41 mmol) in toluene (10 mL) at 20°C in a microwave vial. The reaction mixture was diluted with EtOAc (20 mL) and water (20 mL). The biphasic mixture was filtered through celite. The organic layer was separated and washed sequentially with water (50 mL) and saturated brine (50 mL). The organic layer was filtered and dried over Na2SO4, filtered and evaporated to afford crude product. The crude product was evaporated and was purified by flash silica chromatography, elution gradient 0 to 30% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford (R)-5-(2-(tert- butyldimethylsilyloxy)propylamino)-2-methoxybenzonitrile (0.188 g, 62.2 %) as a orange oil. repated on a lager scale in RSL - See EN04063-90

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-5c2ff1c91b594cd2a9a708b467e463cc
출처 메모750 AstraZeneca ELN dataset