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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 640180생성일: 2026년 10월 24일

Dimethylformamide → 4-(4-Methyl-pyridin-2-yloxymethyl)-benzaldehyde

https://huagongshe.com/ko/reaction/640180

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TetrahydrofuranHCID 8028—
반응물2-(4-Bromo-benzyloxy)4-methyl-pyridineHCID 59255288—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
생성물4-(4-Methyl-pyridin-2-yloxymethyl)-benzaldehydeHCID 5925546755.4%

반응 조건

온도-78 °C

반응 단계

To a tetrahydrofuran (150 mL) solution of 2-(4-bromo-benzyloxy)-4-methyl-pyridine (5.70 g, 20.5 mmol) described in Manufacturing Example 43-1-1 was added dropwise n-butyl lithium (2.67 M n-hexane solution, 9.21 mL, 24.6 mmol) on a dry ice-ethanol bath (−78° C.) under nitrogen atmosphere, which was stirred for 20 minutes at −78° C. N,N-dimethylformamide (3.16 mL, 41.0 mmol) was then added dropwise thereto and stirred for 10 minutes at −78° C. The reaction solution was allowed to room temperature, water was added, and the solution was extracted with ethyl acetate. The organic layer was separated and washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:3) to obtain the title compound (2.58 g, 55.4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691882B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-88d5c0faf7784eff80fe53e639f72f18
출처 메모uspto-grants-2010_04