Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291302Generated: October 31, 2026

Theophylline → 7-[4-[4-(Trifluoromethyl)benzoyl]benzyl]-1,3-dimethylxanthine

https://huagongshe.com/reaction/1291302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTheophyllineHCID 2153—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Trifluoromethylbenzoyl)benzyl bromideHCID 18919118—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product7-[4-[4-(Trifluoromethyl)benzoyl]benzyl]-1,3-dimethylxanthineHCID 1891909036%

Reaction Steps

To a solution of theophylline (1.80 g) in DMF (20 ml) were added potassium carbonate (1.66 g) and 4-[4-(trifluoromethyl)benzoyl]benzyl bromide (3.43 g) and the mixture was stirred at room temperature for 20 hours. This reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with saturated aqueous NaCl solution and dried over anhydrous sodium sulfate and the solvent was distilled off. To the residue was added 4N-hydrogen chloride/ethyl acetate and the resulting precipitate was harvested by filtration. To this precipitate was added a saturated aqueous solution of NaHCO3 and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous NaCl solution and dried over anhydrous sodium sulfate and the solvent was distilled off to provide the title compound as colorless powder (1.57 g, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753664
Source datasetuspto-grants-1998_05
ORD IDord-dade393003cf41e7925cdafdfdde6680
Source noteuspto-grants-1998_05