Reacción #3768

Ecuación de reacción

β-thienyl-D,L-alanine

potassium carbonate

carbobenzyloxychloride

→

N-(Benzyloxycarbonyl) β-thienyl-D,L-alanine

Rendimiento 98.0%

desired compound

Rendimiento 98.0%

Disolventes

H2O

water

dioxane

Condiciones de reacción

Tratamiento posterior

1. 1
   Concentraciónthe reaction mixture was concentrated
2. 2
   OtroThe resultant layers were separated
3. 3
   Lavadothe aqueous layer was washed with 75 mL of diethyl ether
4. 4
   workup.STIRRINGwith rapid stirring to pH=2.0
5. 5
   OtroThe layers were then separated
6. 6
   Secadothe organic layer was dried with sodium sulfate (Na2SO4)
7. 7
   Filtraciónfiltered
8. 8
   Concentraciónconcentrated

Procedimiento

To a mixture of 3.0 g (16.9 mmol) of β-thienyl-D,L-alanine in 75 mL of water and 60 mL of dioxane, was added 5.6 g (40.6 mmol) of anhydrous potassium carbonate, followed by 2.85 mL (20 mmol) of carbobenzyloxychloride. The resulting mixture was stirred rapidly for approximately one hour. When the reaction was substantially complete, as indicated by thin layer chromatography (21/7/7/9, EtOAc/AcOH/CH3 CN/H2O), the reaction mixture was concentrated. The resultant layers were separated and the aqueous layer was washed with 75 mL of diethyl ether and then layered with 150 mL of methylene chloride. The resultant mixture was acidified with rapid stirring to pH=2.0 using 5N hydrochloric acid. The layers were then separated, and the organic layer was dried with sodium sulfate (Na2SO4), filtered and concentrated to provide 5.05 g of desired compound (98%).

Fuente