The reaction of 3-p-nitrophenoxy-3-chlorodiazirine with a 1.1:1.0:1.6 blend of tetrabutylammonium chloride, cesium chloride, and the ionic liquid 1-butyl-3-methylimidazolium chloride at 40-50 degrees C under vacuum at 1 mm.Hg produced a melt from which dichlorodiazirine distilled into a cold trap containing pentane at -70 degrees C over 6-7 h. Dichlorodiazirine, the first nitrogenous precursor for dichlorocarbene, was reasonably stable in the dark at 25 degrees C and efficiently generated the carbene upon photolysis.
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http://dx.doi.org/10.1021/ja055656c | DOI Listing |
J Am Chem Soc
October 2005
Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, New Brunswick, NJ 08903, USA.
The reaction of 3-p-nitrophenoxy-3-chlorodiazirine with a 1.1:1.0:1.
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