Réaction #2446074
ord-838f7654a7c145f6a1656e708286d9d8
Équation de réaction
Réactifs
Solvants
Conditions de réaction
Traitement
- 1Températureto maintain the pH at 8-10
- 2ExtractionThe resulting dark red solution was extracted with ethyl acetate
- 3Concentrationconcentrated
- 4workup.DISSOLUTIONThe residue was dissolved in dichloromethane
- 5Filtrationthe insoluble sodium chloride was filtered
- 6AutrePale yellow crystals formed from the filtrate, which
- 7Autrewere collected
- 8Autredried under vacuum
- 9AutreYield (2.87 g) (11.2 mmol, 42%)
Mode opératoire
2-Chloromethylpyridine hydrochloride (9.2 g, 8.53 mmol) and glycin (2 g, 26.6 mmol) were dissolved in water (30 mL) and stirred at room temperature for five days, with addition of 5 mol aqueous NaOH solution at intervals to maintain the pH at 8-10. The resulting dark red solution was extracted with ethyl acetate, neutralized with HCl and concentrated. The residue was dissolved in dichloromethane, and the insoluble sodium chloride was filtered. Pale yellow crystals formed from the filtrate, which were collected and dried under vacuum. Yield (2.87 g) (11.2 mmol, 42%). 1H NMR (CDCl3), 300 MHz): 3.39 (s, 2H), 3.98 (s, 4H), 7.06 (t, 2H), 7.30 (d, 2h), 7.56 (t, 2H), 8.36 (d, 2H). 13C NMR (CD3OD, 300 MHz): 57.36 (C, CH2), 59.77 (2C, PyCH2), 124.77 (2CH, Py), 125.15 (2CH, Py), 139.00 (C, CH2), 149.76 (2CH, Py), 156.10 (2C, Py), 173.05 (C, CO2H).