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4-CHLORO-4'-PYRROLIDINOMETHYL BENZOPHENONE synthesis

3synthesis methods
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Yield:-

Reaction Conditions:

Stage #1: pyrrolidine;4-bromomethyl-4'-chlorobenzophenonewith potassium carbonate in acetonitrile at 80; for 16 h;
Stage #2: with hydrogenchloride in diethyl ether;water;acetonitrile;
Stage #3: with potassium carbonate in diethyl ether;water;acetonitrile;

Steps:

32

Reference Example 32; (4-chlorophenyl)[4-(1-pyrrolidinylmethyl)phenyl]methanone; [] Acetonitrile (55 ml) was added to [4-(bromomethyl)phenyl](4-chlorophenyl)methanone (6.71 g, 21.7 mmol), potassium carbonate (5.99 g, 43.3 mmol) and pyrrolidine (3.62 ml, 43.3 mmol), and the mixture was stirred at 80°C for 16 hrs. The solvent was concentrated, and diethyl ether was added to the residue. The mixture was extracted with 1N hydrochloric acid. The extract was basified with potassium carbonate, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and the solvent was evaporated under reduced pressure. The obtained residue was purified by alumina column chromatography (developing solvent; ethyl acetate) to give the title compound (4.79 g).

References:

EP1593667,2005,A1 Location in patent:Page/Page column 45-46