Реакция #63991

ord-8a2f92c2d143402187baa2f3871614ad

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияwere filtered
  2. 2
    Концентрированиеthe filtrate concentrated to an oil
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in 400 ml
  4. 4
    Промывкаof ethyl acetate which was washed with a 1% hydrochloric acid solution
  5. 5
    ДругоеThe organic phase was separated
  6. 6
    Сушкаdried over magnesium sulfate
  7. 7
    Концентрированиеconcentrated to an oil
  8. 8
    ДругоеThe residue was triturated with diethyl ether
  9. 9
    Фильтрацияthe resulting solids filtered under nitrogen
  10. 10
    Другоеof the desired product crystallized from the filtrate

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04767743uspto-grants-1988_08