Реакция #214754

ord-dabc0e0b0de24a699e6448bf16b48244

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияAfter completion of the hydrogenation, the catalyst was filtered off
  2. 2
    Другоеthe filtrate was evaporated to dryness

Методика

A solution of 14.3 g of N-(2-chloro-6-nitrobenzyl)-L-alanine ethyl ester in 50 ml of absolute ethanol was hydrogenated in the presence of 1 g of Raney nickel. After completion of the hydrogenation, the catalyst was filtered off and the filtrate was evaporated to dryness. There were obtained 12.6 g (99% of theory) of N-(2-amino-6-chlorobenzyl)-L-alanine ethyl ester; nD22 =1.5430.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04256748uspto-grants-1981_03