Réaction #2286285
ord-3e3311f0edeb4d86921a3b59d9703971
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1TempératureThe reaction mixture was heated
- 2Températureto reflux for 24 h
- 3ConcentrationAt this time, the reaction mixture was concentrated under vacuum
- 4workup.ADDITIONThe resulting solid was diluted with water (100 mL)
- 5Extractionextracted with ethyl acetate (2×50 mL)
- 6workup.ADDITIONThe water layer was acidified to pH=2 by the addition of a 1N aqueous hydrochloric acid solution
- 7Extractionwas extracted with ethyl acetate (2×50 mL)
- 8Lavagewashed with a saturated aqueous sodium chloride solution (50 mL)
- 9Séchagedried with magnesium sulfate
- 10Filtrationfiltered
- 11Concentrationconcentrated under vacuum
- 12AutreThe resulting solid was dried under high vacuum overnight
Mode opératoire
A suspension of (3-chloro-4-hydroxy-5-methyl-phenyl)-acetonitrile (4b) (1.3 g, 0.0071 mol) in water (2.06 mL) was treated with ethylene glycol dimethyl ether (13.93 mL, 0.133 mol) followed by potassium hydroxide (2.8 g, 0.0071 mol). The reaction mixture was heated to reflux for 24 h. At this time, the reaction mixture was concentrated under vacuum. The resulting solid was diluted with water (100 mL) and extracted with ethyl acetate (2×50 mL). The organic layers were discarded. The water layer was acidified to pH=2 by the addition of a 1N aqueous hydrochloric acid solution and was extracted with ethyl acetate (2×50 mL). The organic layers were combined, washed with a saturated aqueous sodium chloride solution (50 mL), dried with magnesium sulfate, filtered and concentrated under vacuum. The resulting solid was dried under high vacuum overnight to afford (3-chloro-4-hydroxy-5-methyl-phenyl)-acetic acid (5b) (1.4 g, 97%) as a white solid; EI(+)-HRMS m/z calcd for C9H9ClO3 (M+) 200.0240, found 200.0247. Molecular Weight=200.6233; Exact Mass=200.0240