16673-84-0Relevant articles and documents
Onium Salt-catalyzed Acylations with Diketene
Dehmlow, Eckehard V.,Shamout, Abdul Rahman
, p. 2062 - 2067 (2007/10/02)
Weak NH- and CH-acids can be acylated advantageously by diketene (1) in the presence of a quarternary ammonium chloride.Carboxamides yield with one or two moles of 1 the products 3 or 10 selectively. β-Keto esters and β-diketones lead to 12a, b or 13, respectively, and acetoacetamides give 5 or 8.The polymer 16 and/or 17 is formed by self-condensation of 1.
Synthesis of N-Acylacetoacetamide using 2,2,6-Trimethyl-1,3-dioxin-4-one
Sato, Masayuki,Kanuma, Norio,Kato, Tetsuzo
, p. 1315 - 1321 (2007/10/02)
Diketene-acetone adduct (2,2,6-trimethyl-1,3-dioxin-4-one) 1 reacts with amide NH to give the corresponding N-acetoacetates 2.Formamide and basic amides such as picolinamide, on treatment with the adduct, are transformed to the N-acyl-2,6-dimethyl-4-oxo-4H-pyran-3-carboxamide (4a and 4p) together with the corresponding N-acetoacetates.Keywords--diketene-acetone adduct; 1,3-dioxin-4-one; acetylketene; diketene; acetoacetylation; 4-pyrone derivatives; N-acylacetoacetamide
Studies on ketene and its derivatives. XVII. Reaction of diketene with imidates.
Kato,Yamamoto
, p. 1334 - 1338 (2007/10/04)
-