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n.1.(Chem.) Any one of several metameric alkaloids, C5H3N.(CH3)2, of the pyridine series, obtained from bone oil as liquids, and having peculiar pungent odors. These alkaloids are also called respectively dimethyl pyridine, ethyl pyridine, etc.
Webster's Revised Unabridged Dictionary, published 1913 by G. & C. Merriam Co.
References in periodicals archive ?
Various oligosaccharides having an N-acetylglucosamine unit at the reducing end such as chitooligosaccharides and N-acetyllactosamine were converted to the corresponding [beta]-glycosyl azides in good yields in the presence of 2,6-lutidine as a base.
The reaction of PC13 with nucleosides in the presence of 2,6-lutidine at low temperature followed by sequential conjugations and final cyclization reaction produced cyclic triphosphotriester compounds containing three nucleosides.
Labes, "Metal nitrate and thiocyanate complexes with 2,6-lutidine N-oxide," Journal of Inorganic and Nuclear Chemistry, vol.
Entry Reaction conditions Time Yield (%) (a) 1 NCS, NaHC[O.sub.3], EtOAc 16 h 43 2 [([Bu.sub.3]Sn).sub.2]O, t-BuOCl, DCM [36] 16 h 11 3 NaOCl, [Et.sub.3]N, DCM 16 h 26 4 NCS, [K.sub.2]C[O.sub.3], EtOAc, [H.sub.2]O 16 h 49 5 CuS[O.sub.4] x 5[H.sub.2]O, L-Ascorbate, 12 h 30 NaHC[O.sub.3], t-BuOH, [H.sub.2]O [37] 6 NaI, 2,6-Lutidine, t-BuOCl, dioxane [38] 12 h 30 7 HTIB, C[H.sub.3]CN [39] 12 h 0 8 NBS, [Et.sub.3]N, DMF [40] 18 h 1 9 Cr[O.sub.2], C[H.sub.3]CN [41] 12 h 18 (a) Determined by analysis of the crude reaction mixture by analytical LC/MS.