Answers are grounded in this paper and cite their sources.
All 7 monomethyl- and all 21 dimethyl-quinolines were synthesized by unambiguous methods and those solid above room temperature were purified to their maximum melting points. The picrates, styphnates, and trinitro-m-cresolates of each quinoline were prepared and their properties recorded. The picrates in particular were purified to their ultimate melting points. Incidentally, 7-ethyl-quinoline and a number of trimethyl-quinolines were also prepared. It is concluded that the melting points previously given in the literature for most of the picrates are of little use for identification purposes.
No takes yet. Share an insight, caveat, or question.
Manske et al. (1942) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: