Synthesis of 2-Aminocarboxylic Acids on the Basis of Metalated Lithium Acylates


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2-Aminocarboxylic acids have been synthesized through the reaction of lithium acylate α-carbanions with alkyl nitrites to form α-hydroxyiminoacylates, followed by reduction of the latter with tin chloride. The reactions of lithium acylate α-carbanions, generated by the metalation of carboxylic acids with lithium diisopropylamide at 35–40°С in THF under argon, with alkyl nitrites at 45–50°С give 2-hydroxyiminocarboxylic acids in 55–97% yields. The reduction of 2-hydroxyiminocarboxylic acids with tin(II) chloride in conc. HCl at 20–25°С leads to 2-aminocarboxylic acid hydrochlorides in 52–94% yields.

作者简介

A. Zorin

Ufa State Petroleum Technological University, ul. Kosmonavtov 1

编辑信件的主要联系方式.
Email: chemist.518@mail.ru
俄罗斯联邦, Ufa, Bashkortostan, 450062

A. Lenkova

Ufa State Petroleum Technological University, ul. Kosmonavtov 1

Email: chemist.518@mail.ru
俄罗斯联邦, Ufa, Bashkortostan, 450062

A. Khachaturyan

Ufa State Petroleum Technological University, ul. Kosmonavtov 1

Email: chemist.518@mail.ru
俄罗斯联邦, Ufa, Bashkortostan, 450062

V. Zorin

Ufa State Petroleum Technological University, ul. Kosmonavtov 1

Email: chemist.518@mail.ru
俄罗斯联邦, Ufa, Bashkortostan, 450062


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