2 Ethyl 2 oxazoline

From propionic acid and derivatives

Carboxylic acids, carboxylic esters, carboxylic amides and nitriles can be reacted with 2-amino alcohols by heating to 200 °C upon dehydration to the corresponding N-(2-hydroxy)carbamide which at 260-280 °C react further upon dehydration to the 2-alkyl-2-oxazoline.

For example N-(2-hydroxyethyl)propionamide is first formed from propionic acid and ethanolamine in 74% yield which can be dehydrated to give 2-ethyl-2-oxazoline in about 75% yield.

Less drastic reaction conditions require the dehydration of the N-(2-hydroxyethyl)propionamide in vacuo in the presence of iron(III)chloride, which delivers the product in 90% yield. An even higher yield of 96.2% is obtained by heating with zinc acetate.

An economic one-pot reaction is heating the salt of propionic acid with ethanolamine at 200 °C in vacuo in the presence of zinc chloride yielding 82% 2-ethyl-2-oxazoline. From the water-containing distillate pure 2-ethyl-2-oxazoline can be isolated by extraction with diethylbenzene and subsequent distillation or by distillation only after addition of diethyl phosphite or dimethyldichlorosilane. The product can be dried to a residual water content of 10 ppm.

In another one-pot reaction propionic acid is converted first with 2-aminoethanol to 2-hydroxyethylamide, than reacted with boric acid at 130 °C yielding a boric acid ester which is finally thermolyzed at 280 °C in 92% yield to 2-ethyl-2-oxazoline.

From propionic acid and thionyl chloride propionyl chloride can be obtained, which reacts with ethanolamine in the presence of an acid scavenger (for example pyridine) to N-propionyl-2-aminoethanol. With further thionyl chloride this reacts further to 2-chloroethylamide. With the chloride ion as a better leaving group, this intermediate is cyclized by simple heating to the oxazoline. Water must be excluded du to the tendency of oxazolines towards ring-opening by chloride ions during protonation of the imine nitrogen.

The direct reaction of propionyl chloride with 2-chloroethylamine hydrochloride in the presence of triethylamine avoids the formation of water.

From propanal

Propanal reacts with 2-aminoethanol in t-butanol to 2-ethyl-2-oxazoline in the presence of the iodinating reagent 1,3-diiodo-5,5-dimethylhydantoin (DIH) and potassium carbonate.

Properties

2-Ethyl-2-oxazoline is a readily water-soluble, colorless liquid which is also soluble in a variety of organic solvents and possesses an amine-like smell. Aqueous solutions react alkaline. The compound is stable in alkaline but hydrolyses under acid action.

Applications

In anhydrous form, 2-ethyl-2-oxazoline is mostly used as a monomer.

The cationic ring-opening polymerization of 2-ethyl-2-oxazoline can be initiated by alkylation with e.g. methyl tosylate or triflates (in particular methyl triflate) and leads to the water-soluble poly(2-ethyl-2-oxazoline) which is a propionyl-substituted linear polyethylenimine and can also be seen as a pseudo-polypeptide.

The polymerization of 2-ethyl-2-oxazoline can also be carried out as living cationic polymerization.

Copolymers with other 2-alkyl-2-oxazolines and other monomers allow the preparation of random copolymers and block copolymers.

The copolymers obtained can be used as biocompatible drug carriers, in coatings and adhesives, and in many other applications.

The elimination of the propionyl group from poly (2-ethyl-2-oxazoline) yields linear polyethyleneimine.