HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-(4-(Trifluoromethyl)benzyloxy)pyridine 1-oxide | HCID 68657649 | — |
| Product | 4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-one | HCID 57950480 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365540B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-5ade6a1d9ba7468caf5ad965a11d205c |
| Source note | uspto-grants-2016_06 |