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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 330생성일: 2026년 10월 23일

1-(Benzyloxy)-4-bromo-2-fluorobenzene → (R)-4-(benzyloxy)-N-(2-(tert-butyldimethylsilyloxy)propyl)-3-fluoroaniline

https://huagongshe.com/ko/reaction/330

반응식

참여 물질

역할이름HCID투입량
반응물1-(Benzyloxy)-4-bromo-2-fluorobenzeneHCID 18757491—
반응물(R)-2-(tert-butyldimethylsilyloxy)propan-1-amineHCID 59302513—
시약Cesium carbonateHCID 10796—
촉매Palladium (II) acetateHCID 4144353—
촉매2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
용매1,4-DioxaneHCID 31275—
생성물(R)-4-(benzyloxy)-N-(2-(tert-butyldimethylsilyloxy)propyl)-3-fluoroanilineHCID 584644350%

반응 조건

온도120 °C

반응 단계

PdOAc2 (0.080 g, 0.36 mmol) and dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (0.170 g, 0.36 mmol) were added in one portion to a degassed solution of 1-(benzyloxy)-4-bromo-2-fluorobenzene (1 g, 3.56 mmol), (R)-2-(tert- butyldimethylsilyloxy)propan-1-amine (0.808 g, 4.27 mmol) and cesium carbonate (1.739 g, 5.34 mmol) in anhydrous dioxane (20 mL) at 20°C in a microwave vial. The microwave vial was sealed and the reaction was heated to 120 °C for 10 hours in the microwave reactor and cooled to RT. LCMS indicates mainly starting material **** No further action was taken.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-1df10534bfeb467c9df72e530f4b3ab2
출처 메모750 AstraZeneca ELN dataset