Reacción #93880

Ecuación de reacción

benzhydrylazidoformate

L-leucine

magnesium oxide

water

→

N-benzhydryloxycarbonyl-L-leucine

Disolventes

dioxane

Condiciones de reacción

Tratamiento posterior

1. 1
   FiltraciónIt is then filtered
2. 2
   Concentraciónthe filtrate is concentrated
3. 3
   Otroto remove the dioxane
4. 4
   ConcentraciónThe aqueous concentrate
5. 5
   Extracciónthe acidified mixture is extracted with ethyl acetate
6. 6
   OtroThe extract is dried
7. 7
   Otroevaporated to dryness

Procedimiento

To a mixture consisting of 13.1 g. of L-leucine, 6 g. of magnesium oxide, and 150 ml. of water is added a solution of 25.3 g. of benzhydrylazidoformate in 150 ml. of dioxane, and the resulting mixture is stirred at room temperature for 2 days. It is then filtered, and the filtrate is concentrated to remove the dioxane. The aqueous concentrate is acidified with solid citric acid, and the acidified mixture is extracted with ethyl acetate. The extract is dried and evaporated to dryness to give an oily residue of N-benzhydryloxycarbonyl-L-leucine, which is suitable for use without further purification. To a mixture of 32 g. of this intermediate product, 25 g. of pentachlorophenol, and 300 ml. of ethyl acetate, at 5° C., is added 20 g. of dicyclohexylcarbodiimide, and the resulting mixture is kept at 5° C. for 5 hours and filtered. The filtrate is concentrated to small volume, and the concentrate is treated with petroleum ether to give a precipitate of N-benzhydryloxycarbonyl-L-leucine pentachlorophenyl ester, which is isolated and crystallized from ethanol-water; m.p. 84°-86° C.; [α]D25 -27.8° (2% in methanol).

Fuente