Reacción #1504307
ord-fa6996ccd0e64dda8e5dd47f43c02f56
Ecuación de reacción
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Reactivos
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Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONwere added at -5° C.
- 2workup.STIRRINGThe resulting mixture was stirred for 24 hours
- 3LavadoThe resulting chloroform solution was successively washed twice with a 10% by weight aqueous citric acid solution
- 4SecadoThereafter, the organic phase was dried over anhydrous sodium sulfate
- 5OtroThe solvent was then completely removed in vacuo
- 6Otroto obtain a white oily material
- 7OtroThis was crystallized from hexane
Procedimiento
In 80 ml of chloroform were dissolved 14.8 g (42 mmol) of t-butyloxycarbonylglycine.dicyclohexylamine and 14.0 g (41.5 mmol) of glycine benzyl ester p-toluenesulfonic acid salt. To this solution, 70 ml of a chloroform solution containing 8.75 g (45.7 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDAC) were added at -5° C. with stirring. The resulting mixture was stirred for 24 hours. The resulting chloroform solution was successively washed twice with a 10% by weight aqueous citric acid solution, then twice with water, then twice with a 4% by weight aqueous sodium hydrogen carbonate solution and finally twice with water. Thereafter, the organic phase was dried over anhydrous sodium sulfate. The solvent was then completely removed in vacuo to obtain a white oily material. This was crystallized from hexane to obtain 12.8 g (yield: 96%) of t-butyloxycarbonyl-glycylglycine benzyl ester as a white solid. In 10 ml of ethyl acetate were dissolved 8.0 g (24.8 mmol) of t-butyl oxycarbonylglycylglycine benzyl ester, to which 120 ml of 4N HCl/ethyl acetate were added. The mixture was stirred for 4 hours and then the solvent was removed in vacuo to obtain white precipitates. The precipitates were washed well with diethyl ether to obtain 6.4 g (yield: 100%) of glycylglycine benzyl ester hydrochloride as a white solid having the following physical properties: