Реакция #214756

ord-aff6cb749c0b4b578c93a3c78a4729ed

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe catalyst was then filtered off
  2. 2
    Другоеthe filtrate was evaporated to dryness

Методика

A solution of 14.3 g of N-(2-chloro-6-nitrobenzyl)-D-alanine ethyl ester in 50 ml of ethanol was hydrogenated in the presence of 1 g of Raney nickel. 3.35 liters of hydrogen were taken up in 2 hours. The catalyst was then filtered off and the filtrate was evaporated to dryness. There were obtained 12.6 g (99% of theory) of N-(2-amino-6-chlorobenzyl)-D-alanine ethyl ester; nD23 =1.5405; [α]D =+55.8° (c=1% in ethanol).

Источник

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