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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1868119생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1868119

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참여 물질

역할이름HCID투입량
반응물2-Bromo-5-fluorobenzotrifluorideHCID 520983—
반응물2-Methylpiperazine, (R)-HCID 7330434—
반응물Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물(R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazineHCID 6855494882.4%

반응 조건

온도100 °C

반응 단계

(R)-2-methyl-piperazine (3.5 g, 34.9 mmol), 2-bromo-5-fluoro benzotrifluoride (7.74 g, 31.7 mmol), BINAP (0.59 g, 0.95 mmol), tBuONa (4.58 g, 47.65 mmol) and Pd2(dba)3 (0.29 g, 0.32 mmol) were mixed in the flask and purged with N2. Anhydrous toluene (50 mL) was added and purged with N2 again. The resulting mixture was heated in an oil bath at 100° C. under N2 for 3 hours. The mixture was cooled to room temperature, diluted with dichloromethane (150 mL), washed with H2O (30 mL) first, then washed with saturated brine (30 mL). The combined organic layer was dried over Na2SO4, concentrated down under reduced pressure to give a brown color liquid as crude. The crude product was purified on silica gel column eluted with 5-10% MeOH in DCM to give (3R)-1-[4-fluoro-2-(trifluoromethyl)phenyl]-3-methylpiperazine as a light yellow oil (6.85 g, 82%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07632838B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-d533b43a677146f8923ac74e7be809ee
출처 메모uspto-grants-2009_12