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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Bromo-5-fluorobenzotrifluoride | HCID 520983 | — |
| 반응물 | 2-Methylpiperazine, (R)- | HCID 7330434 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 촉매 | Binap, (A+-)- | HCID 634876 | — |
| 촉매 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 생성물 | (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine | HCID 68554948 | 82.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07632838B2 |
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| 출처 데이터셋 | uspto-grants-2009_12 |
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| ORD ID | ord-d533b43a677146f8923ac74e7be809ee |
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| 출처 메모 | uspto-grants-2009_12 |
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