Reaktion #220022
ord-a90803229e1048bd8eb8e095c822d434
Reaktionsgleichung
compound
3-Formyl-2-hydroxy-5-trifluoromethylpyridine
sodium formate
hydroxylamine hydrochloride
formic acid
→
desired product
3-Cyano-2-hydroxy-5-trifluoromethylpyridine
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturheated
- 2Temperaturto reflux overnight
- 3TemperaturThe reaction mixture was cooled
- 4workup.WAITto stand at room temperature for 7 d
- 5Extraktionextracted with three portions of ethyl acetate
- 6WaschenThe combined organic layers were washed sequentially with two portions of water, saturated aqueous sodium bicarbonate solution and brine
- 7Trocknendried over sodium sulfate
- 8Einengenconcentrated in vacuo
Vorschrift
A mixture of the compound from Step B above (18 g, 95 mmol), sodium formate (7.1 g, 110 mmol), hydroxylamine hydrochloride (7.3 g, 110 mmol), and formic acid (150 mL) was stirred at room temperature for 2 h and then heated to reflux overnight. The reaction mixture was cooled, allowed to stand at room temperature for 7 d, poured into water and extracted with three portions of ethyl acetate. The combined organic layers were washed sequentially with two portions of water, saturated aqueous sodium bicarbonate solution and brine, dried over sodium sulfate and concentrated in vacuo to yield the desired product as a brown powder. 1H NMR (400 MHz, CD3OD) δ 8.37 (d, J=2.7 Hz, 1H), 8.19 (q, J=0.7 Hz, 0.3 Hz, 1H).