Reacción #63991

Ecuación de reacción

dicyclohexylcarbodiimide

N-t-butoxycarbonyl-L-alanine

D-alanine benzyl ester p-toluenesulfonic acid salt

triethylamine

→

N-t-butoxycarbonyl-L-alanyl-D-alanine benzyl ester

Disolventes

methylene chloride

methylene chloride

Condiciones de reacción

Tratamiento posterior

1. 1
   Filtraciónwere filtered
2. 2
   Concentraciónthe filtrate concentrated to an oil
3. 3
   workup.DISSOLUTIONThe residue was dissolved in 400 ml
4. 4
   Lavadoof ethyl acetate which was washed with a 1% hydrochloric acid solution
5. 5
   OtroThe organic phase was separated
6. 6
   Secadodried over magnesium sulfate
7. 7
   Concentraciónconcentrated to an oil
8. 8
   OtroThe residue was triturated with diethyl ether
9. 9
   Filtraciónthe resulting solids filtered under nitrogen
10. 10
    Otroof the desired product crystallized from the filtrate

Procedimiento

To a solution of 23.0 g. (0.121 m) of N-t-butoxycarbonyl-L-alanine, 42.6 g. (0.121 m) of D-alanine benzyl ester p-toluenesulfonic acid salt and 17 ml. (0.121 m) of triethylamine in 400 ml. of cold (0° C.) methylene chloride was added dropwise 25.0 g. (0.121 m) of dicyclohexylcarbodiimide in 100 ml. of methylene chloride. After stirring overnight at room temperature the solids were filtered and the filtrate concentrated to an oil. The residue was dissolved in 400 ml. of ethyl acetate which was washed with a 1% hydrochloric acid solution, a 10% potassium carbonate solution, water and a brine solution. The organic phase was separated, dried over magnesium sulfate and concentrated to an oil. The residue was triturated with diethyl ether and the resulting solids filtered under nitrogen, 16.0 g. An additional 12.7 g. of the desired product crystallized from the filtrate.

Fuente