10213-75-9Relevant academic research and scientific papers
Catalytic Olefin hydroalkoxylation by nano particles of pollucite
Zamanian, Sara,Kharat, Ali Nemati
, p. 981 - 986 (2015/06/25)
The catalytic hydroalkoxylation of α,β-unsaturated esters, nitriles, and ethers with aliphatic and aromatic alcohols over pollucite using thermal and microwave-assisted methods was investigated. To study the effect of the alcohol structures on the mechanism of the hydroalkoxylation reaction, different alcohols, such as methanol to butanol, cyclohexanol, phenol, and 2-ethylhexanol were used. The activities of pollucite, in contrast to other basic solids, were scarcely affected by the presence of air and moisture. The correlation between alcohol acidity and reaction activity is discussed. The prepared pollucite was characterized by X-ray diffraction, volumetric nitrogen adsorption surface area analysis, and CO2 temperature-programmed desorption. Scanning electron microscopy analysis revealed that the size of the modified nano catalyst particles was under 40nm.
Catalysis of a hydroxyapatite-bound Ru complex: Efficient heterogeneous oxidation of primary amines to nitriles in the presence of molecular oxygen
Mori,Yamaguchi,Mizugaki,Ebitani,Kaneda
, p. 461 - 462 (2007/10/03)
A hydroxyapatite-bound Ru complex could efficiently catalyze the aerobic oxidation of various primary amines to nitriles which were further hydrated to amides in the presence of water.
A simple and convenient method for the synthesis of nitriles by oxidation of primary amines with NaOCl in ethanol
Yamazaki, Shigekazu
, p. 3559 - 3564 (2007/10/03)
The oxidation of aliphatic primary amines having α-methylene on treatment with NaOCl as an oxidant in ethanol has been found to be an effective method for the transformation of primary amines to nitriles.
Nickel-catalyzed dehydrogenation of amines to nitriles
Yamazaki,Yamazaki
, p. 301 - 303 (2007/10/02)
Aliphatic primary amines having α-methylene underwent oxidative dehydrogenation on treatment with NiSO4 as a catalyst and K2S2O8 as an oxidant to give the corresponding nitriles in good yields. Benzhydrylamine was converted to benzhydrylideneamine quantitatively under the same reaction conditions.
