37484-68-7Relevant academic research and scientific papers
Acylation of Ketone Silyl Enol Ethers with Acid Chlorides. Synthesis of 1,3-Diketones
Tirpak, Robin E.,Rathke, Michael W.
, p. 5099 - 5102 (2007/10/02)
Trimethylsilyl enol ethers of ketones are acylated by a variety of acid chlorides in the presence of zinc chloride or antimony trichloride.The major product of this reaction is the 1,3-diketone resulting from C-acylation.Some O-acylation is observed in most cases.Yields of 1,3-diketones varied but were usually good to excellent.
Preparation of 1,3-Diketones and of Nitro-diketones by (1:1)-Acylation of Lithium Enolates with Acyl Chlorides
Seebach, Dieter,Weller, Thomas,Protschuk, Gerd,Beck, Albert K.,Hoekstra, Marvin S.
, p. 716 - 735 (2007/10/02)
Slow addition of precooled solutions of lithium enolates in THF to solutions of equimolar amounts of acyl chlorides in the same solvent at temperatures between -80 and -100 deg furnishes 1,3-diketones in acceptable to good yields.Even 3-nitropropionyl and 4-nitrobutyryl chloride can be employed for the (1:1)-acylation of enolates to give the synthetically useful 5- and 6-nitro-1,3-diketones 13 and 25, respectively.The scope and the limitations of this method of preparing 1,3-diketones are given and are compared with alternative methods.
