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5-METHYL-2-(4-TRIFLUOROMETHOXYPHENYL)-3H-IMIDAZOLE-4-CARBOXYLIC ACID ETHYL ESTER synthesis

1synthesis methods
93919-56-3 Synthesis
4-(TRIFLUOROMETHOXY)BENZYLAMINE

93919-56-3
155 suppliers
$10.00/1g

5408-04-8 Synthesis
ETHYL 2-(HYDROXYIMINO)-3-OXOBUTANOATE

5408-04-8
65 suppliers
$32.00/500mg

5-METHYL-2-(4-TRIFLUOROMETHOXYPHENYL)-3H-IMIDAZOLE-4-CARBOXYLIC ACID ETHYL ESTER

868851-35-8
17 suppliers
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Yield:-

Reaction Conditions:

in acetonitrile; for 17 h;Heating / reflux;

Steps:

1 Preparation of 5-methyl-2-(4-trifluoromethoxy-phenyl)-1H-imidazole-4-carboxylic acid ethyl ester

To a solution of 7.9 g of ethyl 2-oximinoacetoacetate in acetonitrile (100 ml) was added 10.5 g of 4-(trifluoromethoxy)benzylamine (as R4-CH2-NH2). The reaction mixture was then refluxed for 17 hours under argon atmosphere. After such time the reaction mixture was cooled down to 0° C., the solid was filtered off, washed with acetonitrile, and dried in vacuo to yield 11.2 g of a light yellow powder, MS (ISP) 315 (M+H)+.

References:

US2005/250769,2005,A1 Location in patent:Page/Page column 14

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