HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 3-octyl-6-(4-octyloxyphenyl)-1H-2-pyridone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-octyl-2-(4-octyloxyphenyl)pyridine N-oxide | HCID 54368283 | — |
| Product | 3-octyl-6-(4-octyloxyphenyl)-1H-2-pyridone | HCID 19046956 | — |
Reaction Steps
2.20 g (5.4 mmol) of 5-octyl-2-(4-octyloxyphenyl)pyridine N-oxide are refluxed in 30 ml of acetic anhydride for 4 hours. The acetic anhydride is then distilled off, and the residue is taken up in 10 ml of 1:1 methylene chloride/methanol, and the mixture is stirred with methanolic potassium hydroxide solution for 1 hour. Washing with water and concentrated ammonium chloride solution, drying over sodium sulfate, filtration, removal of the solvent by distillation and recrystallization from 8:2 n-hexane/ethyl acetate give 1.79 g of 3-octyl-6-(4-octyloxyphenyl)-1H-2-pyridone. ##STR14##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05630962 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-9356afaf2f2f43f28739f6c2a4db3e1d |
| Source note | uspto-grants-1997_05 |