Abstract
(2-Pyridylamino)diethylborane has been obtained in good yield and purity by the reaction of triethylborane with 2-aminopyridine in 2 1 molar ratio in the absence of solvent. Carbon-13 NMR data suggest that at room temperature and below the compound exists in at least two forms; only at higher temperatures does the normal aminoborane form become exclusive. Pyrolysis of the compound leads to the formation of B-triethyl- N-tri-2-pyridylborazine, [BC 2H 5N(2-CHN)] 3.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
