Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Tetralin oxime

A three-necked round-bottom flask is fitted with a dropping funnel, a thermometer, and a magnetic stirrer and is heated in a water bath to 30°. Tetralin (1.32 g, 0.01 mole) and 50 ml of 3.5 Anitric acid solution are placed in the flask and brought to temperature. Ceric ammonium nitrate (21.9 g, 0.04 mole) is dissolved in 100 ml of 3.5 N nitric acid, and the solution is added dropwise to the reaction mixture at a rate such that the temperature does not rise and only a pale yellow color is evident in the reaction mixture. At the completion of the reaction (1 to 2 hours), the mixture should be colorless. The solution is cooled to room temperature, diluted with an equal volume of water, and extracted twice with ether. The ether solution is dried with anhydrous sodium sulfate, filtered, and the ether is evaporated. The residue may be distilled to yield a-tetralone (bp 113-11676 mm or 170749 mm) or may be converted directly to the oxime, which is recrystallized from methanol, mp 88-89°. [Pg.14]

Tetralin 2-Amino-1-oxo- IV/lc, 541 (Oxim-Red.) XI/1, 904 (Oxim/ Amino-Keton-Umlag.)... [Pg.741]


See other pages where Tetralin oxime is mentioned: [Pg.763]    [Pg.4]    [Pg.149]    [Pg.385]    [Pg.4]    [Pg.645]   
See also in sourсe #XX -- [ Pg.14 ]




SEARCH



Tetraline

Tetralines

© 2024 chempedia.info