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HRID 77897생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/77897

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 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-a322369c707e495283faa3205c06efcf
출처 메모uspto-grants-2014_09