2- ethanol 3-Methoxyethyl acetate

Methoxy ether of propylene glycol. See Methor isopropanol 2-(2-Methoxyethox] ethanol. See Methor iglycol 2-(2-(2-Methoxyethox] ethox] ethanol. See Triglycol monomethyl ether Methoxyethyl acetate 2-Methoxyethyl acetate Methoiqrethyl acetate. 

Methoxyethanol) see Methyl glycol (2-(2-Methoxyethoxy)ethanol) see Methyldiglycol (2-Methoxyethyl acetate) see Methyl glycol acetate (Methoxyethylene) see Methyl vinyl ether... 

After 8 hours boiling of solution of 3.8 g of 3 -nitro-benzylideneacetoacetic acid isopropylester, 8 grams of acetoacetic acid p-metoxyethyl ester and 6 ml cone ammonia in 80 ml ethanol under reflux, 2,6-dimethyl-4-(3 -nitrophenyl)-1,4-dihydropyridine 3-p-methoxyethyl ester 5-isopropyl ester of melting point 125°C (petroleum ether/ acetic ester) was obtained. Yield 49% of theory. 

The complexes are very soluble in methanol, ethanol, butanol, methyl Cellosolve (2-methoxyethanol), and ethyl Cellosolve (2-ethoxyethanol), and to a fair degree, quite soluble in 1,2-dimethoxyethane and di- and triglyme. They are initially quite soluble in tetrahydrofuran, acetone, pyridine, nitro-methane, acetonitrile, dimethyl sulfoxide, and iV,A/-dimethyl-formamide, but usually precipitation of the nickel halide-solvent complex occurs if attempts are made to prepare moderately concentrated solutions in these solvents. They are only very slightly soluble, or are quite insoluble in dioxane, ethyl ether, hexane, dichloromethane, ethyl acetate, and methyl- and butyl-cellosolve acetate (2-methoxyethyl and 2-butoxyethyl acetate). 

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