114-91-0

Usage

Uses

Used in Pharmaceutical Industry:
2-(2-Methoxyethyl)pyridine is used as a solvent for the production of various pharmaceuticals, facilitating the manufacturing process and improving the solubility of active ingredients.
Used in Pesticide Industry:
In the pesticide sector, 2-(2-Methoxyethyl)pyridine serves as a solvent, aiding in the formulation of effective pest control products by enhancing the solubility and stability of the active ingredients.
Used in Rubber Industry:
2-(2-Methoxyethyl)pyridine is utilized as a solvent in the rubber industry, contributing to the production of rubber products by ensuring the proper mixing and processing of raw materials.
Used in Chemical Synthesis:
2-(2-Methoxyethyl)pyridine is employed as a precursor in the synthesis of bioactive compounds, indicating its potential role in the development of new pharmaceuticals and other bioactive substances.

InChI:InChI=1/C8H11NO/c1-10-7-5-8-4-2-3-6-9-8/h2-4,6H,5,7H2,1H3

Upstream product

• 110-86-1 pyridine 
• 67-56-1 methanol 
• 74-85-1 ethene 
• 100-69-6 2-vinylpyridine 
• 110-67-8 3-Methoxypropionitrile 
• 74-86-2 acetylene 
• 1121-60-4 pyridine-2-carbaldehyde 

Downstream Products

• 1185088-10-1 2-(2-methoxyethyl)piperidine hydrochloride 
• 6311-84-8 2-[2-(pyrrol-1-yl)ethyl]pyridine 
• 1228934-56-2 (4S)-4-(1H-indazol-3-ylmethyl)-6-{2-[2-(2-methoxyethyl)piperidin-1-yl]-2-oxoethyl}-1-phenyl-4H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepin-5(6H)-one 
• 1228935-20-3 benzyl 2-(2-methoxyethyl)piperidine-1-carboxylate 
• 2116-62-3 2-(2-phenylethyl)pyridine 
• 100-69-6 2-vinylpyridine 

Relevant academic research and scientific papers

Catalytic Amination of β-(Hetero)arylethyl Ethers by Phosphazene Base t-Bu-P4

We describe the catalytic amination of β-(hetero)arylethyl ethers with amines using the organic superbase t-Bu-P4 to obtain β-(hetero)arylethylamines. The reaction has a broad substrate scope and allows the transformations of electron-deficient and electron-neutral β-(hetero)arylethyl ethers with various amines including pyrrole, N-alkylaniline, diphenylamine, aniline, indole, and indoline derivatives. Mechanistic studies indicate a two-reaction pathway of MeOH elimination from the substrate to form a (hetero)arylalkene followed by the hydroamination of the alkene.

First Cobalt(I)-catalysed Heterocyclotrimerization of Ethyne with Nitriles to Pyridines in Water under Mild Conditions

In water the synthesis of substituted pyridines with cobalt(I)-complexes is carried out at room temperature and normal pressure with very high product selectivity in the presence of light.

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.

Alkylation of Pyridine in Free Radical Chain Reactions Utilizing Alkylmercurials

Pyridines or N,N,N',N'-tetramethyl-p-phenylenediamine will undergo a photostimulated free radical chain reaction with alkylmercury halides or carboxylates, yielding ring alkylated substitution products.Alkene mercuration products (R1CH(Y)CH(R2)HgX with Y=HO, RO, CH3CONH; X=Cl, CH3CO2, CF3CO2) can be used without isolation for the alkylation reaction

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.