تفاعل #63991

ord-8a2f92c2d143402187baa2f3871614ad

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحwere filtered
  2. 2
    تركيزthe filtrate concentrated to an oil
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in 400 ml
  4. 4
    غسيلof ethyl acetate which was washed with a 1% hydrochloric acid solution
  5. 5
    أخرىThe organic phase was separated
  6. 6
    تجفيفdried over magnesium sulfate
  7. 7
    تركيزconcentrated to an oil
  8. 8
    أخرىThe residue was triturated with diethyl ether
  9. 9
    ترشيحthe resulting solids filtered under nitrogen
  10. 10
    أخرىof the desired product crystallized from the filtrate

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04767743uspto-grants-1988_08