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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Theophylline | HCID 2153 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Trifluoromethylbenzoyl)benzyl bromide | HCID 18919118 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-[4-[4-(Trifluoromethyl)benzoyl]benzyl]-1,3-dimethylxanthine | HCID 18919090 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753664 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-dade393003cf41e7925cdafdfdde6680 |
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| Source note | uspto-grants-1998_05 |
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