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1-(3,4-DICHLOROPHENYL)-2-(1H-IMIDAZOL-1-YL)ETHANONE synthesis

3synthesis methods
-

Yield:37906-39-1 60%

Reaction Conditions:

in acetonitrile at 0; for 3.5 h;

Steps:

69.1 Step 1: Preparation of 1-(3,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethanone

After dissolving 1 g of 3,4-dichlorophenacyl bromide in 10 mL of acetonitrile, 762 mg of imidazole was added at 0° C., followed by stirring for 2 h and 1.5 h at rt. The solvent was removed, the residue was washed with water, extracted with MC, dried over MgSO4, and concentrated. After adding diethyl ether, it was solidified with hexane.Yield: 578 mg (60%, yellow solid)

References:

KR2021/52042,2021,A Location in patent:Paragraph 0685-0690

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