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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1186356생성일: 2026년 10월 26일

(Trifluoromethyl)trimethylsilane → 2-(Pyrrolidin-1-yl)-5-(2,2,2-trifluoro-1-hydroxyethyl)-pyridine

https://huagongshe.com/reaction/1186356

반응식

참여 물질

역할이름HCID투입량
반응물(Trifluoromethyl)trimethylsilaneHCID 552549—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물6-(Pyrrolidin-1-yl)pyridine-3-carbaldehydeHCID 2794775—
용매TetrahydrofuranHCID 8028—
생성물2-(Pyrrolidin-1-yl)-5-(2,2,2-trifluoro-1-hydroxyethyl)-pyridineHCID 6740173694%

반응 단계

According to Reference Example 8-12, by use of 6-(pyrrolidin-1-yl)-3-pyridinecarboxaldehyde (173 mg, 0.982 mmol), (trifluoromethyl)trimethylsilane (174 μL, 1.18 mmol), tetrabutylammonium fluoride (a 1.0 mol/L solution in tetrahydrofuran, 98.0 μL, 0.098 mmol) and tetrahydrofuran (5.0 mL), the mixture was stirred and reacted at room temperature for 30 minutes. Then, slurry purification was performed using hexane, to give 2-(pyrrolidin-1-yl)-5-(2,2,2-trifluoro-1-hydroxyethyl)-pyridine (Compound DH) (227 mg, yield: 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08673908B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-fd9eef4168e448158e86ec565aff527f
출처 메모uspto-grants-2014_03