40195-48-0Relevant academic research and scientific papers
Synthesis of 16-aryl-15-oxadispiro[5.1.5.3]hexadecane-7,14-diones by reformatsky reaction
Kirillov,Nikiforova,Vasyanin,Dmitriev
, p. 513 - 517 (2015/05/20)
Abstract Methyl 1-bromocyclohexanecarboxylate reacted with zinc and aromatic aldehydes in two steps to afford 16-aryl-15-oxadispiro[5.1.5.3]hexadecane-7,14-diones; methyl 1-[aryl(hydroxy)methyl]cyclohexanecarboxylates were also formed as by-products.
Reformatsky synthesis of 16-aryl-15-oxadispiro[5.1.5.3]-hexadecane-7,14-diones
Kirillov,Shchepin
, p. 1223 - 1224 (2007/10/03)
Methyl 1-bromocyclohexanecarboxylate reacts with zinc in the presence of cyclohexanecarbonyl chloride to give methyl 1-(cyclohexylcarbonyl)cyclohexanecarboxylate. Treatment of the latter with bromine leads to formation of methyl 1-(1-bromocyclohexylcarbonyl)cyclohexanecarboxylate which reacts with zinc and aromatic aldehydes, yielding 16-aryl-15-oxadispiro[5.1.5.3]hexadecane-7,14-diones.
