HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535785Generated: October 31, 2026
Diethyl Ether → Methyl 3-(trifluoromethyl)pyrazine-2-carboxylate
https://huagongshe.com/reaction/535785
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Methyl chlorodifluoroacetate | HCID 73935 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Methyl 3-iodopyrazine-2-carboxylate | HCID 57681180 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-(trifluoromethyl)pyrazine-2-carboxylate | HCID 58542464 | 41% |
Reaction Steps
To methyl 3-iodopyrazine-2-carboxylate (7) (10 g, 37.88 mmol) in DMF (Volume: 300 mL) was added methyl chlorodifluoroacetate (27 g, 0.189 mol), potassium fluoride (13.2 g, 0.227 mol), and copper chloride (22.47 g., 0.227 mol). The reaction was heated at 120° C. for 12 h. The reaction mixture was poured into ethyl ether (1000 ml) and washed with brine (3×300 ml), dried over MgSO4 before the solvent was removed. The residue was loaded onto a silica column and was eluted using ethyl acetate/hexanes gradient to afford the title compound (3.19 g, 41%) as an amber oil: 1H NMR (400 MHz, CDCl3) δ 8.85 (d, J=5.4 Hz, 1H), 8.82 (d, J=5.4 Hz, 1H), 4.05 (s, 3H); EIMS m/z 206.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859558B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-63bf36e5f48d40acb54f35fe0f53d70e |
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| Source note | uspto-grants-2014_10 |
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