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ChemicalBook CAS DataBase List 1-Ethyl-3-methylimidazolium bromide

1-Ethyl-3-methylimidazolium bromide synthesis

5synthesis methods
-

Yield:111-55-7 90%

Reaction Conditions:

at 20; for 3 h;Inert atmosphere;

Steps:

2
Example 1 and 2: ethylene glycol diacetate; A 100 mL Schlenk flask was equipped with a magnetic stirring bar, EMIM-acetate (50.0 g, 0.293 mol), and 0.5 equivalents of 1,2-dichloroethane (14.5 g, 0.146 mol) were added at room temperature and reaction was stirred at 70°C for 3h. After reaction two phases were obtained upper layer was decanted and the reaction mixture was extracted 3 times with diethyl ether, all fractions were combined and diethyl ether was removed under vacuum. The final pure product was obtained as color less liquid (90.0% yield) When 1, 2-dibromoethane was used as substrate the reaction was very fast even at room temperature and was highly exothermic. The reaction proceeds via homogeneous pathway; the pure product was distilled from the reaction mixture at 100°C under reduced pressure (90.0% yield). Ethylene glycol diacetate: 1H NMR (CDCl3, 400.13 MHz): δ = 2.02 (s, 6 H, CH3), 4.2 (s, 4H, CH2); 13C NMR: δ = 20.9 (CH3), 62.3 (CH2), 170.9 (CO); FTIR (ATR mode): v = 2961 (br), 1735 (s), 1371 (m), 1213 (s), 1048 (m).

References:

BASF SE;Universität Siegen Institut für Anorganische Chemie EP2532646, 2012, A1 Location in patent:Page/Page column 5-7

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