67267-86-1Relevant academic research and scientific papers
ONE-STEP SYNTHESIS OF KETONES FROM CARBOXYLIC ACIDS AND GRIGNARD REAGENTS IN THE PRESENCE OF A NICKEL(II)-PHOSPHINE CATALYST.
Fiandanese, V.,Marchese, G.,Ronzini, L.
, p. 3677 - 3680 (1983)
A one-step synthesis of diaryl and alkyl-aryl ketones by the reaction of carboxylic acid with Grignard reagents in the presence of NiCl2(Ph2PCH2CH2PPh2) as catalyst is described.In the nickel-catalyzed Grignard reaction the formation of alcohols is nearly completely suppressed.
Synthesis of Trialkylacetic Acids by the Anodic Oxidation of 3,3-Disubstituted-2-oxo Carboxylic Acids
Rabjohn, Norman,Cranor, W. L.,Schofield, C. M.
, p. 1732 - 1736 (2007/10/02)
The "non-Kolbe" electrolysis of 3,3-disubstituted-2-oxocarboxylates 1-3 in methanol produced mixtures of methyl trialkylacetates 5, trialkylacetaldehydes 6, in some cases 2-hydroxy-3,3,3-trialkylpropionic acids 7, trialkylethylenes 8, and methyl trialkylmethyl ethers 9.When one of the substituents on the 3-carbon of the 2-oxo carboxylate was phenyl 4, molecular rearrangement was not observed.In addition to products 5-9, with the exception of 7, there was obtained with 4 an alkyl phenyl ketone 10.The methyl trisubstituted acetates were saponified to the desired trialkylacetic acids.
