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Acetic Anhydride → 4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | 4-(4-(Trifluoromethyl)benzyloxy)pyridine 1-oxide | HCID 68657649 | — |
| 生成物 | 4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09365540B2 |
| 出典データセット | uspto-grants-2016_06 |
| ORD ID | ord-5ade6a1d9ba7468caf5ad965a11d205c |
| 出典メモ | uspto-grants-2016_06 |