Abstract
A systematic investigation of the synthesis of dl-valine by the Strecker method, starting from isobutyraldehyde, has been made. The potassium-cyanide–ammonium-chloride procedure, as modified by us, has been found to be the most convenient for the large scale laboratory preparation of this amino acid, considering the over-all yield, the purity of the amino acid, and the time required, as well as the ease of preparation. A continuous ether extraction of the amino nitrile has been introduced. This accounts for the high yield and easy separation of the pure amino acid.
Publisher
Canadian Science Publishing
Subject
Pharmacology (medical),Complementary and alternative medicine,Pharmaceutical Science
Cited by
13 articles.
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