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HRID 2202842作成日:2026年10月27日

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

https://huagongshe.com/reaction/2202842

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物4-(4-(Trifluoromethyl)benzyloxy)pyridine 1-oxideHCID 68657649—
生成物4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-oneHCID 57950480—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09365540B2
出典データセットuspto-grants-2016_06
ORD IDord-5ade6a1d9ba7468caf5ad965a11d205c
出典メモuspto-grants-2016_06