HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Oxo-5-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | 2-Oxo-5-(trifluoromethyl)-1,2-dihydropyridine-3-carbaldehyde | HCID 19819669 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 2-Oxo-5-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile | HCID 14837020 | — |
Reaction Steps
A solution of 3-formyl-5-trifluoromethyl-2-pyridone (3.5g) (UK Application No. 89310162.6), hydroxylamine hydrochloride (1.42g) and sodium formate (1.39g) in 98% formic acid (42ml) was heated to reflux for a period of 20 hours. After cooling to ambient temperature, the reaction mixture was poured into water, and rigorously extracted with ethyl acetate. The combined organic extracts were washed with saturated aqueous sodium bicarbonate solution, followed by brine, and dried over anhydrous magnesium sulphate. Removal of the solvent under reduced pressure gave 3-cyano-5-trifluoromethyl-2-pyridone as an off-white solid which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05109004 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-0ceb31faf03640279030ee5124879cc2 |
| Source note | uspto-grants-1992_04 |