HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424974Generated: October 29, 2026
Cesium fluoride → 2,2,2-Trifluoro-1-(pyrazin-2-yl)ethan-1-one
https://huagongshe.com/reaction/424974
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | Methyl pyrazinoate | HCID 72662 | — |
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2,2,2-Trifluoro-1-(pyrazin-2-yl)ethan-1-one | HCID 57930527 | — |
Reaction Steps
Pyrazine carboxylate methyl ester (7 g) was dissolved in dimethoxy ethane (monoglyme) (20 mL) and treated at room temperature with trimethylsilyltrifluoro-methane (10 mL; 1.44 eq) and caesium fluoride (0.77 g; 0.1 eq) that had been freshly dried at for 10 minutes under vacuum while being heated with a heat gun. After 18 hours at room temperature the reaction mixture was concentrated under reduced pressure at room temperature, and the residue was dissolved in tetrahydrofuran (50 mL) and acetic acid (20 mL) and treated with tert-butylammonium fluoride (50 mL; 1M THF solution) for 3 hours at room temperature. The reaction was diluted with ethyl acetate, and washed with dilute aqueous sodium bicarbonate solution (3 times), brine, dried over anhydrous sodium sulfate, and evaporated to dryness under reduced pressure to an oil. Trituration of the oil with dichloromethane/hexane gave 2,2,2-trifluoro-1-(pyrazin-2-yl)ethanone (18) as a brown solid (2.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106059B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-cd8fa047526b42489c58111452331654 |
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| Source note | uspto-grants-2012_01 |
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