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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229854Generated: October 31, 2026

4-(Trifluoromethoxy)benzylamine → Ethyl 5-methyl-2-[4-(trifluoromethoxy)phenyl]-1H-imidazole-4-carboxylate

https://huagongshe.com/reaction/229854

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethoxy)benzylamineHCID 571846—
ReactantHCID 178472877HCID 178472877—
SolventAcetonitrileHCID 6342—
ProductEthyl 5-methyl-2-[4-(trifluoromethoxy)phenyl]-1H-imidazole-4-carboxylateHCID 5340440271.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563910B2
Source datasetuspto-grants-2009_07
ORD IDord-887971a452514cba90cd6752ffff4cf7
Source noteuspto-grants-2009_07