돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1811891생성일: 2026년 10월 27일

Trifluoroacetic acid → 2-Fluoro-5-(4-(methylthio)benzyl)pyridine

https://huagongshe.com/reaction/1811891

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물TriethylsilaneHCID 12052—
반응물(6-Fluoropyridin-3-yl)(4-(methylthio)phenyl)methanolHCID 59548286—
용매DichloromethaneHCID 6344—
생성물2-Fluoro-5-(4-(methylthio)benzyl)pyridineHCID 5954836689%

반응 단계

A solution of (6-fluoropyridin-3-yl)(4-(methylthio)phenyl)methanol (1.716 g, 6.88 mmol) in DCM (3.0 mL) was treated with trifluoroacetic acid (2.56 mL, 34.4 mmol) resulting in a green solution. The mixture was stirred for 5 min, and then triethylsilane (3.30 mL, 20.65 mmol) was added dropwise. The green color dissipated rapidly to give a straw colored solution, and a brief exotherm was observed (DCM started refluxing). The mixture was stirred for 30 min, and then extracted into DCM from saturated aqueous NaHCO3. The DCM extracts were dried (MgSO4) and purified by flash chromatography (5% to 7.5% EtOAc/hexane) to give 2-fluoro-5-(4-(methylthio)benzyl)pyridine (89% over 2 steps) as a colorless oil. 1H NMR (400 MHz, d6-DMSO) δ 8.15 (s, 1H); 7.81 (t, J=8.22 Hz, 1H); 7.20 (s, 4H); 7.10 (d, J=8.41 Hz, 1H); 3.94 (s, 2H); 2.44 (s, 3H). 19F NMR (376 MHz, d6-DMSO) 6-72.37 (s, 1 F). m/z (ESI, +ve ion) 234.0 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08362241B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-c573ac0b82bf40e08066981f09e47a5c
출처 메모uspto-grants-2013_01