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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84464생성일: 2026년 10월 24일

Dimethylformamide → 3-Iodo-4-(2-(thiophen-3-yl)ethoxy)pyridine

https://huagongshe.com/ko/reaction/84464

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물Thiophene-3-ethanolHCID 83731—
반응물4-Chloro-3-iodopyridineHCID 2763163—
용매WaterHCID 962—
생성물3-Iodo-4-(2-(thiophen-3-yl)ethoxy)pyridineHCID 5790021181%

반응 단계

To a solution of 4-chloro-3-iodo-pyridine (4.79 g, 20.0 mmol) and 2-(3-thienyl)ethanol (2.43 mL, 22.0 mmol) in a mixture of tetrahydrofuran (60 mL, 700 mmol) and N,N-dimethylformamide (20 mL, 200 mmol) was added sodium hydride, 60% dispersion in mineral oil (0.960 g, 24.0 mmol) portionwise over 30 min. The mixture was stirred for 2 hours, poured carefully into 200 ml of cold water and extracted with diethylether twice. The organic extract was washed with water and brine, and dried over MgSO4. After concentration under vacuum, the crude residue was purified on silica gel column, eluting with 50% ethyl acetate in hexane to give 3-iodo-4-(2-(thiophen-3-yl)ethoxy)pyridine (yield 5.34 g, 81%). 1H NMR (400 MHz, CDCl3) δ 8.75 (s, 1H), 8.35 (d, J=5.6, 1H), 7.29 (dd, J=3.0, 4.8, 1H), 7.19 (s, 1H), 7.12 (d, J=4.9, 1H), 6.70 (d, J=5.6, 1H), 4.26 (t, J=6.5, 2H), 3.21 (t, J=6.5, 2H). MS (ESI+) 332.0, 221.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846762B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c9a50cfa59594005bbfad5c0ea478f83
출처 메모uspto-grants-2014_09