Its diisopropylaminoethanol, and some diphenylacetic acid. Got my eyes on some Hunig's base, given the non-nucleophilic nature of diisopropylethylamine, then conversion to the bromide or iodide, tosylate etc. and hydrogenation ought to do the trick, no? Especially using a good leaving group like tosylate, brosylate or nosylate. As for the diphenylacetic acid then I'll leave what thats for to the imagination. And the ones behind it are a tub of sodium dichromate, and bottles of n-butyric anhydride (if ever a reagent was a real pleasure to work with....then you'll LOVE butryic anhydride
), propionyl chloride, benzoyl chloride and trans-cinnamyl chloride. The bottles and containers wrapped in an outer layer are 2-pyrollidone (been thinking maybe some racetams, phenylpiracetam super cheap, would be rather neat, from what I've heard of it. Had good results with pramiracetam, but so far haven't tried phenylpiracetam. Phenylaniracetam, phenylpramiracetam etc. might be interesting candidates to explore) and I think one of them might be borohydride. The one with the darker inside and the full wrapping tied on is 2-pyrollidone, and the greyish thing behind the sodium is a can of NaBH4, or rather, the metal can the bottle came in, with the bottle sealed inside, the outside purged with argon and a covering stuck over the top, although my borohydride should have a pretty good shelf life, as its in the form of convenient 1g-per-piece tablets rather than powder. (not that those would be 'tablets' anybody would want to swallow xD )
And its covered in mineral oil, its just surface oxidation, the actual inner lining has been vac/heatsealed by the manufacturer, no change observed since it first came, and if one squeezes it etc. then there is clearly a slightly thick fluid over the surface, doubtless some sort of kerosene, mineral spirits etc. And its in an outer bag full of some inert gas. And getting (and keeping) the surface of a block of alkali metal pristine shiny is...well it takes melting and ampouling under inert atmosphere, skimming any oxide layer off and then sealing it under inert gas, I don't think I've ever seen a lab-supply of sodium metal that doesn't come in sealed vials that doesn't have some oxidation on the surface. And I have had that particular block a year or two, and it still looks just as it did when it came in the post (I've often thought...I REALLY wouldn't like to be a postie, out in filthy weather and the freezing cold come what may. But being MY postman....I'd be looking for a new job
)
I don't expect it to stay fresh and shiny very much when supplied, even in oil etc. there will be a degree of surface oxidation. And since I first obtained it and until now, there hasn't been any visible.
And, you missed the other oxidation state of the alkali metals. -1. The alkalides. Kinda neat IMO, even forming a sodium hydride where the negative charge is on the Na atom. Aka 'inverse sodium hydride', the alkali metal behaving as the anion whilst the H bears the positive charge, prepared using cryptand ligands followed by a metathesis rxn to give Na-H+, that have some some similarity to electrides. Always thought it might be fun to attempt the synthesis. And using dimethyl ether as a solvent for extraction and crystallization, how convenient is that? since MeOMe just boils off as if it were hardly there to begin with, especially if it were done with vacuum after purging the system with inert gas, quickest solvent crystallization EVER.
(still got to get the last couple of pieces of my rotavap sent)
Finally getting the pork off my arse too it seems. Started a case against them and planning to take it all the way (and after what they have done lately, IMO they are going to be ankle deep in dogshit after I've finished. From the neck up