Reacción #4528
ord-0c0661338a584907b09ee85e49489e40
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otro(approximately 10 min)
- 2workup.STIRRINGthe mixture is stirred for 6 hours at 20° C
- 3Extracciónthe mixture is extracted with 2×20 ml of ethyl acetate
- 4Extracciónextracted with 3×30 ml of ethyl acetate
- 5LavadoThe extract is washed with saturated NaCl solution
- 6Secadodried over MgSO4
- 7Otroevaporated
- 8OtroThe product obtained
- 9Otrois crystallised in ethyl acetate
Procedimiento
To a solution of 1.33 g (10 mmol) of L-aspartic acid in a dioxane/water (1:1) mixture (30 ml), 4.2 ml (30 mmol) of triethylamine are added, and the mixture is stirred until solution is complete (approximately 10 min). 2.85 g (10 mmol) of tert-butyl 1,2,2,2-tetrachloroethyl carbonate are then added and the mixture is stirred for 6 hours at 20° C. 50 ml of water are then added and the mixture is extracted with 2×20 ml of ethyl acetate. The aqueous phase is acidified (pH 2-3) with NHCl, and then extracted with 3×30 ml of ethyl acetate. The extract is washed with saturated NaCl solution, dried over MgSO4 and evaporated. The product obtained is crystallised in ethyl acetate and petroleum ether. 1.4 g (60% yield) of the expected acid is obtained. ##STR60##