Reacción #214895

ord-202369a7eef443ae976c9ed556f237df

Ecuación de reacción

N[C@@H](CC(=O)O)C(=O)O
L-Aspartic acid
[Na+].[OH-]
sodium hydroxide
CCSC(=S)OC
Methyl ethyl xanthate
CO
methanol
CCOC(=S)N[C@@H](CC(=O)O)C(=O)O
N-ethoxythiocarbonyl-L-aspartic acid
Rendimiento 89.0%

Disolventes

Condiciones de reacción

Temperatura
45°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled to room temperature
  2. 2
    Lavadowashed with two portions of ethylene dichloride
  3. 3
    Otroacidified with concentrated hydrochloric acid at 0° C
  4. 4
    Extracciónextracted with two portions of ethyl acetate
  5. 5
    SecadoThe organic extracts were dried over anhydrous magnesium sulfate
  6. 6
    Otroevaporated in vacuo

Procedimiento

L-Aspartic acid (19.95 g, 0.150 mol) was suspended in 15 ml of water at 0° C., and 50% sodium hydroxide solution (24 g, 0.30 mol) was added dropwise with stirring. Methyl ethyl xanthate (22.44 g, 0.165 mol) in 15 ml of methanol was then added in one portion. The mixture was heated at 45° C. for 2 hours, cooled to room temperature, and washed with two portions of ethylene dichloride. The ethylene dichloride washes were discarded and the aqueous phase acidified with concentrated hydrochloric acid at 0° C. The solution was saturated with solid sodium chloride and extracted with two portions of ethyl acetate. The organic extracts were dried over anhydrous magnesium sulfate and evaporated in vacuo to afford 29.4 g (89%) of white crystalline N-ethoxythiocarbonyl-L-aspartic acid. mp 133° C.; nmr (DMSO-d6) δ1.23 (t, 3H, J=7 Hz), 2.67 (d, 2H, J=6 Hz), 4.37 (q, 2H, J=7 Hz), 4.93 (dt, 1H, J=6 Hz, 8 Hz), 9.26 (d, 1H, J=8 Hz).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04256897uspto-grants-1981_03