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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2202842생성일: 2026년 10월 27일

Acetic Anhydride → 4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-one

https://huagongshe.com/reaction/2202842

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물4-(4-(Trifluoromethyl)benzyloxy)pyridine 1-oxideHCID 68657649—
생성물4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-oneHCID 57950480—

반응 단계

A solution of 4-((4-(trifluoromethyl)benzyl)oxy)pyridine 1-oxide (350 mg) in acetic anhydride (6 ml) was heated under reflux for 4 h. The reaction mixture was then cooled to room temperature and concentrated in vacuo. The residue was diluted with MeOH (10 ml) and 2 M NaOH (10 ml), and heated at reflux for 1 h. The reaction mixture was cooled to room temperature and concentrated in vacuo. The residue was diluted with water and extracted with DCM. The DCM layer was concentrated in vacuo and purified by silica gel column chromatography (MeOH/DCM) to give the title compound (110 mg) as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09365540B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-5ade6a1d9ba7468caf5ad965a11d205c
출처 메모uspto-grants-2016_06