60766-10-1Relevant academic research and scientific papers
Synthesis and structure of copper(II) 3-(3′,5′-di-tert-butyl- 4′-hydroxybenzyl)acetylacetonate
Pod''yachev,Bukharov,Litvinov,Morozov,Gubaidullin,Nugumanova,Mukmeneva
, p. 1651 - 1657 (2004)
Copper(II) 3-(3′,5′-di-tert-butyl-4′-hydroxybenzyl) acetylacetonate was prepared, and its molecular and crystal structure were determined by single crystal X-ray diffraction. There are two crystallographically independent molecules of the complex in the c
Salts of acyl halides and 3,5-di-tert-butyl-4-hydroxy-N,N-dimethylbenzylamine in benzylation reactions
Gorbunov, D. B.,Ershov, V. V.,Nikiforov, G. A.
, p. 481 - 485 (2007/10/02)
The interaction of 3,5-di-tert-butyl-4-hydroxy-N,N-dimethylbenzylamine with various acyl halides has been studied.The N-acyl quaternary salts obtained can be used to introdice a sterically hindered phenol fragment into organic compounds containing an active methylene group.
Chemical process
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, (2008/06/13)
Novel bis(3',5'-mono or dihydrocarbyl-4'-hydroxybenzyl)-1,3-diketones are prepared by reacting a (3',5'-mono or dihydrocarbyl-4'-hydroxybenzyl)-1,3-diketone with an N,N-dihydrocarbyl-2,6-mono or dihydrocarbyl-4-aminomethylphenol and an alkyl halide in the presence of an alkaline earth metal halide. The products are useful as antioxidants.
Chemical process for preparing 1,3 diketones
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, (2008/06/13)
Novel (3',5'-dihydrocarbyl-4'-hydroxybenzyl)-1,3-diketones are prepared by reacting an N,N-dihydrocarbyl-2,6-dihydrocarbyl-4-aminomethylphenol with a 1,3-diketone in the presence of a basic substance. The products are useful as antioxidants.
Method of preparing phenolic antioxidants by condensing active methylene compounds with 3,5-di-tert alkyl-4-hydroxybenzylpyridinium salts
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, (2008/06/13)
3,5-Di-tert alkyl-4-hydroxybenzylpyridinium salts are reacted under basic conditions with compounds containing active methylene groups to form phenolic antioxidants. For example, 3,5-di-tert.butyl-4-hydroxybenzylpyridinium chloride is reacted with 2-nitro
