Reacción #78373
ord-9df58f27be494a008558a7642fc4fe3b
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1ExtracciónThe solution was extracted with ethyl acetate (10×25 ml)
- 2ExtracciónThe organic phase was extracted with saturated aqueous sodium chloride
- 3Secadodried over magnesium sulfate
- 4Otroevaporated to dryness, in vacuo
Procedimiento
3-(1-Thyminyl)-propanoic acid methyl ester (1.0 g, 0.0047 mol) was suspended in 2 M sodium hydroxide (15 ml), boiled for 10 min. The pH was adjusted to 0.3 with conc. hydrochloric acid. The solution was extracted with ethyl acetate (10×25 ml). The organic phase was extracted with saturated aqueous sodium chloride, dried over magnesium sulfate, and evaporated to dryness, in vacuo, to give the title compound as a white solid (0.66 g, 71%). M.p. 118-121° C. Anal. for C8H10N2O4, found (calc.) C, 48.38 (48.49) H, 5.09 (5.09); N, 13.93 (14.14). The compound showed satisfactory 1H and 13C-NMR spectra.