HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477435Generated: October 30, 2026
Sodium Iodide → Benzyl 4-(2,2,2-trifluoroethoxy)phenyl ketone
https://huagongshe.com/reaction/477435
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethanol, 2,2,2-trifluoro-, 1-(4-methylbenzenesulfonate) | HCID 67942 | — |
| Reactant | Benzyl 4-hydroxyphenyl ketone | HCID 75607 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 4-(2,2,2-trifluoroethoxy)phenyl ketone | HCID 13881621 | — |
Reaction Steps
A mixture of benzyl 4-hydroxyphenyl ketone (12.5 g; 0.059 mol), potassium carbonate (11.2 g; 0.08 mol) and sodium iodide (0.5 g) in dimethylformamide (80 ml) was heated to 130° C. At this temperature, 2,2,2-trifluoroethyl p-toluenesulphonate (16.4 g; 0.066 mol), dissolved in dimethyl sulphoxide (30 ml), was added dropwise over 30 minutes. It was then stirred for 45 minutes at a 130° C. After cooling, the reaction mixture was poured into ice-water (500 ml) and the precipitate separated. This was recrystallised from diisopropyl ether/hexane to give pure benzyl 4-(2,2,2-trifluoroethoxy)phenyl ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04888340 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-56516d223db747e3a9fa16272e1e4e3d |
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| Source note | uspto-grants-1989_12 |
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