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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545363Generated: October 29, 2026

[5-Bromo-3-methyl-2-(3-trifluoromethoxy-phenyl)-3H-imidazol-4-yl]-methanol → 5-Bromo-3-methyl-2-(3-trifluoromethoxy-phenyl)-3H-imidazole-4-carbaldehyde

https://huagongshe.com/reaction/545363

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[5-Bromo-3-methyl-2-(3-trifluoromethoxy-phenyl)-3H-imidazol-4-yl]-methanolHCID 67133350—
CatalystHCID 178418406HCID 178418406—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-3-methyl-2-(3-trifluoromethoxy-phenyl)-3H-imidazole-4-carbaldehydeHCID 86626031—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2.80 g (8.0 mmol) of [5-bromo-3-methyl-2-(3-trifluoromethoxy-phenyl)-3H-imidazol-4-yl]-methanol in 120 ml of EtOAc was treated in small portions with 4.85 g (55.8 mmol) of manganese(IV) oxide; the reaction mixture was stirred at RT for 2 hours and at 50° C. for 5 hours, it was then cooled down to RT and filtered (with the aid of dicalite) and the solvents were evaporated to give 2.813 g (quant.) of the title compound as colorless oil. MS: 349.0 (MH+, 1Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935707B2
Source datasetuspto-grants-2011_05
ORD IDord-c45c67801fe64005b0285ccebca03b8d
Source noteuspto-grants-2011_05