97190-47-1Relevant academic research and scientific papers
An improved protocol for the preparation of 2,6-di(tert-butyl)-4-methylphenyl (BHT) alkanoates
Evans,Stanley
, p. 515 - 519 (2007/10/02)
Treatment of the acid chloride derivatives 2a-e with potassium 2,6-di(tert-butyl)-4-methyl phenoxide 1b afforded the corresponding BHT esters 3a-e in 83-95% yield.
Acylation and Esterification of the Aryloxide Ligand in . Crystal Structures of , Hbhmap and O=C(dbmp)But (Hdbmp = 2,6-di-tert-butyl-4-methylphenol, Hbhmap = 3-tert-butyl-2-hydroxy-5-methylacetophenone)
Power, Michael B.,Bott, Simon G.,Bishop, Elizabeth J.,Tierce, Kelli D.,Atwood, Jerry L.,Barron, Andrew R.
, p. 241 - 247 (2007/10/02)
The reaction of (Hdbmp = 2,6-di-tert-butyl-4-methylphenol) with O=C(Cl)Me leads to acylation of one of the dbmp ligands and affords 1 (Hbhmap = 3-tert-butyl-2-hydroxy-5-methylacetophenone).Hydrolysis of 1 yields uncomplex
