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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 502732생성일: 2026년 10월 25일

Methyl iodide → 2-(1-Methylpiperidin-3-yl)-5-(trifluoromethyl)benzenamine

https://huagongshe.com/reaction/502732

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물3-(2-Nitro-4-(trifluoromethyl)phenyl)pyridineHCID 46316762—
촉매Adams' catalystHCID 345198—
용매AcetoneHCID 180—
용매BenzeneHCID 241—
용매MethanolHCID 887—
생성물2-(1-Methylpiperidin-3-yl)-5-(trifluoromethyl)benzenamineHCID 58711919—

반응 단계

To an orange solution of 3-(2-nitro-4-(trifluoromethyl)phenyl)pyridine (1.4 g, 5.2 mmol) in 2 ml acetone and 1 mL benzene was added iodomethane (1.0 ml, 16 mmol). The solution was allowed to stand for 5 days, and was concentrated in vacuo to give an orange solid. A portion of this material was treated with platinum (IV) oxide (0.11 g, 0.49 mmol) in 5 ml MeOH under an atmosphere of hydrogen for approximately 24 h. The reaction was flushed with nitrogen, filtered through celite, and concentrated. Purification by silica gel chromatography (MC/MeOH/conc. NH4OH) provided the title compound. MS (m/z): 259.0 (M+H)+. Calc'd for C13H17F3N2: 258.28.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07776869B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-dda1087bd25d4938b7af3b541eb56ea4
출처 메모uspto-grants-2010_08