Reacción #9801

ord-e9f0bef708674089b4baba65dc3ddbb7

Ecuación de reacción

[Na+].[OH-]
NaOH
N[C@@H](CC(=O)O)C(=O)O
aspartic acid
[NH4+].[OH-]
NH4OH
N[C@@H](CC(=O)O)C(=O)O
aspartic acid
N[C@@H](CC(=O)O)C(=O)O
aspartic acid
N[C@@H](CC(=O)[O-])C(=O)[O-].[NH4+].[NH4+]
ammonium aspartate
N[C@@H](CC(=O)[O-])C(=O)[O-].[Na+].[Na+]
sodium aspartate

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.DISTILLATIONdistilled water

Procedimiento

A sample of 13.3 g (100 mmol) of aspartic acid was slurried in 100 ml distilled water with stirring, and the aspartic acid was partially neutralized with 5 ml of 10 N NaOH (50 mmol). Conc. NH4OH (3.38 ml, 14.8 N, 50 mmol) was pipetted into the beaker, fully neutralizing and solubilizing the aspartic acid. The beaker was placed in a drying oven at 120° C. overnight, producing a clear, slightly yellowish glass of the comonomers, aspartic acid (plus residual ammonium aspartate) and sodium aspartate. The beaker was then heated in a vacuum oven at 200° C., 25 mm Hg, for 4 hours, to convert the material to a copolymer of sodium aspartate and succinimide. Titration data confirmed the 1:1 residue ratio.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091305B2uspto-grants-2006_08