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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 499생성일: 2026년 10월 23일

2-Bromo-5-fluorobenzotrifluoride → (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine

https://huagongshe.com/ko/reaction/499

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참여 물질

역할이름HCID투입량
반응물2-Bromo-5-fluorobenzotrifluorideHCID 520983—
반응물2-Methylpiperazine, (R)-HCID 7330434—
시약Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물(R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazineHCID 6855494859%

반응 조건

온도100 °C

반응 단계

1-bromo-4-fluoro-2-(trifluoromethyl)benzene (5 g, 20.58 mmol), (R)-2-methylpiperazine (2.164 g, 21.61 mmol), sodium tert-butoxide (3.95 g, 41.15 mmol) and BINAP (0.512 g, 0.82 mmol) in anhydrous toluene (60 mL) was degassed under vacuum with inlet of nitrogen. TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.377 g, 0.41 mmol) was added, the mixture again degassed. The resulting suspension was stirred at 100 °C for 6 hours under nitrogen. LCMS: Product formed. Cooled and evaporated. Residue diluted with diethyl ether (75 mL), filtered through Celite and the filtrates extracted with 2M HCl (2x30 mL). The combined aqueous layers were basified with solid NaOH to pH ~10, extracted with diethyl ether (2x50 mL), the organic extracts washed with water (2x10 mL) and brine, dried over mgSO4, filtered and evaporated to give crude product (3.2g, 59%) as an orange oil which was used without further purification.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-5ffc5c4a730b4c9fa67430c9657da268
출처 메모750 AstraZeneca ELN dataset