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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 533936생성일: 2026년 10월 25일

N-Methoxy-N-methylacetamide → 1-[5-(Benzyloxy)pyridin-2-yl]ethan-1-one

https://huagongshe.com/reaction/533936

반응식

참여 물질

역할이름HCID투입량
반응물N-Methoxy-N-methylacetamideHCID 537505—
반응물5-(Benzyloxy)-2-bromopyridineHCID 16094696—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-[5-(Benzyloxy)pyridin-2-yl]ethan-1-oneHCID 23143439—

반응 단계

A mixture of 5-benzyloxy-2-bromo-pyridine (1.0 g), N-methoxy-N-methyl-acetamide (780 mg) and THF (20 mL) under argon at −60° C. was added n-BuLi (2.6 M in toluene, 2.9 mL). After 1 hour the cooling bath was removed. After reaching room temperature the mixture was quenched by addition of saturated NH4Cl-solution. The mixture was distributed between EA and brine. The organic phase was dried (Na2SO4), filtered and concentrated. The residue was purified by chromatography (silica gel, heptane to EA/heptane 3:7) to provide the subtitle compound. MS ESI+: m/z=228 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853412B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-0ad92eb2b4a949a0b9cee903a9e4631e
출처 메모uspto-grants-2014_10