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・ 2-Bromopropane
・ 2-Butanol
・ 2-Butene
・ 2-Butoxyethanol
・ 2,5-Dimethoxybenzaldehyde
・ 2,5-Dimethylfuran
・ 2,5-Dimethylhexane
・ 2,5-dioxopiperazine hydrolase
・ 2,5-dioxovalerate dehydrogenase
・ 2,5-Diphenyloxazole
・ 2,5-Furandicarboxylic acid
・ 2,5-Xylidine
・ 2,500 year celebration of the Persian Empire
・ 2,6-beta-fructan 6-levanbiohydrolase
・ 2,6-Di-tert-butylphenol
2,6-Di-tert-butylpyridine
・ 2,6-Diacetylpyridine
・ 2,6-Diaminopurine
・ 2,6-Dichlorobenzonitrile
・ 2,6-Dichlorophenol
・ 2,6-Dihydroxybenzoic acid
・ 2,6-dihydroxypseudooxynicotine hydrolase
・ 2,6-Dihydroxypyridine
・ 2,6-dihydroxypyridine 3-monooxygenase
・ 2,6-Dimethoxybenzoquinone
・ 2,6-Dimethylnaphthalene
・ 2,6-Dimethylpiperidine
・ 2,6-dioxo-6-phenylhexa-3-enoate hydrolase
・ 2,6-Lutidine
・ 2,6-Naphthalenedicarboxylic acid


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2,6-Di-tert-butylpyridine : ウィキペディア英語版
2,6-Di-tert-butylpyridine

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2,6-Di-''tert''-butylpyridine is an organic compound with the formula (Me3C)2C5H3N. This colourless, oily liquid is derived from pyridine by replacement of the two H atoms with tert-butyl groups. It is a hindered base.〔Rafael R. Kostikov, Sánchez-Sancho Francisco, María Garranzo and M. Carmen Murcia "2,6-Di-t-butylpyridine" Encyclopedia of Reagents for Organic Synthesis 2010. 〕 For example, it can be protonated, but it does not form an adduct with boron trifluoride.
==Preparation==
2,6-Di-''tert''-butylpyridine is prepared by the reaction of tert-butyllithium with pyridine.〔Edward Deutsch, Nai Kong V. Cheung "Noncoordinating buffers. I. Synthesis and characterization of water soluble derivatives of 2,6-di-tert-butylpyridine" ''J. Org. Chem'' 1973, vol 38, pp 1123–1126. 〕 The synthesis is reminiscent of the Chichibabin reaction.
Some related bulky pyridine compounds have been described, including 2,4,6-tri-t-butylpyridine.〔Francis V. Scalzi, Norman F. Golob "Alkylation of pyridine with tert-butyllithium. Convenient syntheses of 2,6-di-tert-butylpyridine and 2,4,6-tri-tert-butylpyridine" ''J. Org. Chem'' 1971, vol 36, pp 2541–2542 . Hongmei Li "2,4,6-Tri-tert-butylpyridine" Encyclopedia of Reagents for Organic Synthesis 2004. 〕 and 2,6-di-tert-butyl-4-methylpyridine.〔Alexandru T. Balaban "2,6-Di-tert-butyl-4-methylpyridine (DTBMP)" Encyclopedia of Reagents for Organic Synthesis 2004. 〕

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