28672-54-0

Usage

Uses

Used in Pharmaceutical Industry:
2-(2-Ethoxyethyl)pyridine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be incorporated into the development of new drugs, potentially enhancing their efficacy and properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(2-Ethoxyethyl)pyridine serves as a key intermediate in the production of various agrochemicals. Its ability to be integrated into the molecular structures of these compounds contributes to their effectiveness in agricultural applications.
Used in Dye Production:
2-(2-Ethoxyethyl)pyridine is utilized as a chemical intermediate in the synthesis of dyes. Its presence in the molecular structure of dyes can influence their color, stability, and other properties, making it an important component in the dye industry.
Used as a Solvent:
Due to its solubility properties, 2-(2-Ethoxyethyl)pyridine is used as a solvent in various chemical processes. Its ability to dissolve a wide range of substances makes it a valuable asset in the chemical industry.
Used as a Corrosion Inhibitor:
2-(2-Ethoxyethyl)pyridine is employed as a corrosion inhibitor, protecting materials from the damaging effects of corrosion. Its application in this area helps to extend the lifespan of various industrial equipment and structures.
Used in Specialty Coatings and Adhesives:
As a component in specialty coatings and adhesives, 2-(2-Ethoxyethyl)pyridine contributes to the performance and properties of these materials. Its inclusion can enhance their durability, adhesion, and other characteristics, making it a useful additive in these formulations.
While 2-(2-Ethoxyethyl)pyridine has a relatively low toxicity, it is essential to exercise caution and follow proper safety procedures when handling 2-(2-ETHOXYETHYL)PYRIDINE to minimize potential health risks.

InChI:InChI=1/C9H13NO/c1-2-11-8-6-9-5-3-4-7-10-9/h3-5,7H,2,6,8H2,1H3

Upstream product

• 100-69-6 2-vinylpyridine 
• 64-17-5 ethanol 
• 141-52-6 sodium ethanolate 
• 140-29-4 phenylacetonitrile 
• 123-31-9 hydroquinone 
• 2141-62-0 3-(ethoxy)propionitrile 
• 74-86-2 acetylene 
• 67-64-1 acetone 

Relevant academic research and scientific papers

Evidence of a borderline region between E1cb and E2 elimination reaction mechanisms: A combined experimental and theoretical study of systems activated by the pyridine ring

We report a combined experimental and theoretical study to characterize the mechanism of base-induced β-elimination reactions in systems activated by the pyridyl ring, with halogen leaving groups. The systems investigated represent borderline cases, where it is uncertain whether the reaction proceeds via a carbanion intermediate (E1cb, AxhDH + DN) or via the concerted loss of a proton and the halide (E2, AND EDN) upon base attack. Experimentally, the Taft correlation for H/D exchange, in OD-/D2O with noneliminating substrates (1-methyl-2-(2-Xethyl)pyridinium iodide), is used to predict the expected values of the rate constants for the elimination reactions with N-methylated substrates and F, Cl, Br as the leaving group. The comparison indicates an E1cb irreversible mechanism with F, but the deviation observed with Cl and Br does not allow a conclusive assignment. The theoretical calculations show that for the N-methylated substrate with a fluoride leaving group the elimination proceeds via formation of a moderately stable carbanion. No stable anionic intermediate is instead found when the leaving group is Cl or Br, as well as for any of the nonmethylated species, indicating a concerted elimination. The methylated substrate with Cl shows however only a moderate increase in reactivity compared to the fluorinated substrate, despite the change in mechanism. Very interestingly, our analysis of the computed two-dimensional potential energy surface for the reaction with a F leaving group indeed evidences the lack of a net distinction between the E1cb and E2 reaction paths, which appear to merge smoothly into each other in these borderline cases.

Photoinduced Alkoxylation of 2-Vinylpyridinium Ion

Photoirradiation of 2-vinylpyridine in acidic methanol afforded methyl 2-(2-pyridyl)ethylether in a high yield.Reactions in acetic ethanol and 2-propanol also provided the corresponding alkoxyl derivatives along with a considerable amount of 2-ethylpyridine.It was suggested that photoinduced intramolecular charge-shift from the pyridinium ion moiety into the vinyl group initiates the regioselective nucleophilic addition of alcohol.

SYNTHESIS OF FUNCTIONALLY SUBSTITUTED PYRIDINES AND DIPYRIDYL-SUBSTITUTED COMPOUNDS WITH THE AID OF LOW-VALENCE COMPOLEXES

The possibility of the preparation of oxygen, nitrogen, and sulfur-containing pyridines and dipyridyl-substituted compounds by the cyclocotrimerization of substituted propionitriles with acetylene under the influence of a Co(2-ethylhexanoate)2-Al(C2H5)3 catalyst was demonstrated.It was established that the nature of the heteroatom in substituted propionitriles has virtually no effect on the direction of the reaction.