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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172326Generated: November 1, 2026

Hexane → HCID 89815318, compound

https://huagongshe.com/reaction/2172326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-3-fluorobenzotrifluorideHCID 142414—
Reactant2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
ReactantHCID 178418800HCID 178418800—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 89815318HCID 8981531814.1%

Reaction Conditions

Temperature180 °C

Reaction Steps

A solution of 4-methyl-1H-imidazole (1.352 g, 16.46 mmol) in 20 mL THF was treated with lithium tert-butoxide 1N in hexane (16.46 ml, 16.46 mmol) and was allowed to stir for one hour. The reaction mixture was concentrated and then transferred to a microwave vial charged with 1-bromo-2-fluoro-4-(trifluoromethyl)benzene (2.360 ml, 16.46 mmol) and 10 mL dioxane. The reaction mixture was heated to 180° C. in a microwave reactor for one hour. After cooling to room temperature, the reaction mixture was poured into saturated NH4Cl solution and was extracted with DCM. The organics were concentrated. then purified directly by silica gel column chromatography (0 to 50% EtOAc/heptane) yielding 1-(2-bromo-5-(trifluoromethyl)phenyl)-5-methyl-1H-imidazole (0.710 g, 2.327 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051311B2
Source datasetuspto-grants-2015_06
ORD IDord-7f2dc17dfc6c44d88e911825509fa931
Source noteuspto-grants-2015_06