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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1868126생성일: 2026년 10월 27일

Toluene → (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine

https://huagongshe.com/reaction/1868126

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물alpha,alpha,alpha,3-TetrafluorotolueneHCID 67867—
반응물2-Methylpiperazine, (R)-HCID 7330434—
반응물Sodium t-butoxideHCID 23676156—
촉매Binap, (A+-)-HCID 634876—
용매DichloromethaneHCID 6344—
생성물(R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazineHCID 6855494833.6%

반응 조건

온도110 °C

반응 단계

(R)-2-methyl-piperazine (3.88 g, 38.70 mmol), 2-bromo, 5-fluoro benzotrifluoride (8.55 g, 35.18 mmol), tris(dibenzylidineacetone)dipalladium (0) (32.0 mg g, 0.35 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (657.0 mg, 1.06 mmol) and sodium tert-butoxide (5.07 g, 52.77 mmol) were charged to a reaction flask. Toluene (40 mL) was introduced under nitrogen atmosphere and the reaction mixture was heated up at 110° C. for 5.0 hours. Reaction was complete as determined by TLC. The reaction mixture was diluted with dichloromethane, washed with water, saturated brine then dried over MgSO4 and concentrated. The crude product was purified via flash column chromatography to yield (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine as a light brown oil (3.1 g, 33.6% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07632838B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-9fadd48193674f86aee2834e1273fc9f
출처 메모uspto-grants-2009_12