Hmm, here’s a quick little puzzle that I’m in the middle of solving. If anyone knows the answer, feel free to let me know.

Attempting to make the acid chloride of 2-picolinic acid by SOCl2. In dichloromethane, combined ~5g of 2-picolinic acid with a slight excess of SOCl2 (~1.2:1), refluxed for ~20 minutes, removed solvent, set it aside. The initial solid was tan-brown. After a few days, it was dark. Massively dark. And green-blue, as far as the eye can tell. After a week, it’s bone dry and still massively dark. A rough yield of around 6g. So it picked up some mass…

Solubility testing… Very soluble in water, forms a deep purple solution. Soluble in methanol, solution is a bit more blue. Very slightly soluble in chloroform, purple solution. Very slightly soluble in acetonitrile, greenish leaning toward blue solution.

NMR (in D2O)… Four clean aromatic signals, consistent with the 4 protons of an ortho-substituted pyridine ring, nothing else.


UV-Vis (in water)… Peak at ~540nm, shoulder at ~650nm. Strong peak at ~260nm.

20140204uvvis01 20140204uvvis02

This has not been exhaustively lit searched yet, but the intensity of the color of the product is intriguing AND a ~20% mass increase makes it a fun little puzzle. We will be exploring more…

Open Notebooking/Live Blogging/#RealTimeChem

This is a new experiment for me. Inspired by a number of factors, my research students and I will be keeping open lab notebooks of the research we do at Minnesota State University Moorhead. This will allow everyone to see the great work we do here and will be a good way to keep ourselves up-to-date. The majority of the work posted here will be tentative and some of it may end up being just plain wrong, but that’s one of the exciting parts of science.