RUS  ENG
Full version
JOURNALS // Uspekhi Khimii // Archive

Usp. Khim., 1993 Volume 62, Issue 8, Pages 796–812 (Mi rcr1120)

This article is cited in 6 papers

Methods of synthesis of acrolein and its α-substituted derivatives

N. A. Keiko, M. G. Voronkov

Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences

Abstract: The methods of synthesis of acrolein and its α-alkyl-substituted derivatives are examined: (a) catalytic oxidation of propene, isobutene, propane, isobutane, propyl and tert-butyl alcohols, tert-butyl alkanoates, propionaldehyde, isobutyraldehyde, and allyl alcohol and its ethers: (b) condensation of formaldehyde with aliphatic aldehydes by the Mannich reactions and also in the vapour phase over heterogeneous catalysts. Both general methods (the Mannich reaction, ipso-substitution of a α-halogen in the acrylic system, and interaction of 1-brom-2-ethoxycyclopropyllithium with electrophiles) and various special methods are used in the synthesis of the α, β-unsaturated aldehydes with functional-group-substitutents. The bibliography includes 323 references.

UDC: 547.383

Received: 21.03.1993

DOI: 10.1070/RC1993v062n08ABEH000045


 English version:
Russian Chemical Reviews, 1993, 62:8, 751–767

Bibliographic databases:


© Steklov Math. Inst. of RAS, 2024