0000000000676007
AUTHOR
Pekka Autio
Chlorination of p-cymene by chlorine in carbon tetrachloride: Model compounds for environmental analyses
p-Cymene was chlorinated by chlorine in CCl4. The products of the chlorination were separated by distillation and purified by preparative gas chromatography. The structures of chlorocompounds were confirmed by means of their NMR and mass spectra. The distillation gave as the main compounds: (2) 2-chloro-, (4) 2,3-dichloro-, (5) 2,5-dichloro-, (6) 2,3,6-trichloro-, (7) 2,3,5,6-tetrachloro-p-cymenes and as by-products: (8) 2,5,7-trichloro-p-cymene, (9) 2,6-dichloro-1-methyl-4-(1-methylethenyl)benzene (cymenene), and (10) 2,3,6-trichloro-1-methyl-4-(1-methylethenyl)benzene (cymenene).
A new synthesis and crystal structure of n-(2-hydroxyethyl)succinimide
Abstract N-(2-Hydroxyethyl) succinimide was formed with 80 % yield in the reaction of 2-oxazolidinone with succinic anhydride at 210° C instead of polyesteramides obtained from N-substituted 2-oxazolidinones. The identification based on the crystal structure determination.