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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 726생성일: 2026년 10월 24일

Benzene, 1-bromo-3-(trifluoromethyl)- → 1-[3-(Trifluoromethyl)phenyl]piperidin-4-ol

https://huagongshe.com/ko/reaction/726

반응식

참여 물질

역할이름HCID투입량
반응물Benzene, 1-bromo-3-(trifluoromethyl)-HCID 9817—
반응물Piperidin-4-olHCID 79341—
시약Cesium carbonateHCID 10796—
촉매Binap, (A+-)-HCID 634876—
촉매Palladium (II) acetateHCID 4144353—
용매1,4-DioxaneHCID 31275—
생성물1-[3-(Trifluoromethyl)phenyl]piperidin-4-olHCID 301830943.09%

반응 조건

온도100 °C

반응 단계

A mixture of 1-bromo-3-(trifluoromethyl)benzene (6.13 mL, 44.44 mmol), piperidin-4-ol (5.608 g, 55.44 mmol), diacetoxypalladium (0.200 g, 0.89 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.553 g, 0.89 mmol) and cesium carbonate (18.10 g, 55.55 mmol) in dioxane (100 mL) was evacuated and backfilled with N2 three times and then it was heated at 100 °C for 6h. The mixture was filtered through filter agent(supercell), washed with EtOAc. The combined filtrate was concentrated. The residue was purified by silica gel column(0-35% EtOAc/hexane) to give 1-(3-(trifluoromethyl)phenyl)piperidin-4-ol (4.70 g, 43.1 %) as a yellow oil. 1H NMR (400 MHz, DMSO-d6) d 7.38 (t, _J_ = 8.03 Hz, 1H), 7.20 (dd, _J_ = 2.38, 8.41 Hz, 1H), 7.13 (s, 1H), 7.00 (d, _J_ = 7.78 Hz, 1H), 4.64 - 4.72 (m, 1H), 3.53 - 3.72 (m, 3H), 2.93 (ddd, _J_ = 3.01, 9.98, 12.86 Hz, 2H), 1.71 - 1.88 (m, 2H), 1.45 (dtd, _J_ = 3.89, 9.44, 12.86 Hz, 2H). LCMS 246.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-9afd80193ebe4d909351826d5e746d73
출처 메모750 AstraZeneca ELN dataset