HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972107Generated: October 31, 2026
Ethyl vinyl ether → 3-(Trifluoromethyl)pyrazole
https://huagongshe.com/reaction/1972107
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | Trifluoroacetyl chloride | HCID 61106 | — |
| Reactant | Hydrazinium chloride | HCID 115031 | — |
| Reactant | (3E)-4-Ethoxy-1,1,1-trifluoro-3-buten-2-one | HCID 5709222 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Trifluoromethyl)pyrazole | HCID 1807034 | — |
Reaction Steps
To a solution of 4.4 moles hydrazine.hydrochloride in 2.2 L of methanol in a 3-necked flask, equipped with a mechanical stirrer, a reflux condenser and a dropping funnel an equimolar amount of ETFBO which had been manufactured by addition of trifluoroacetyl chloride to ethyl vinyl ether was added dropwise over about 4 hours under N2 atmosphere. The temperature of the reaction mixture was kept below 15° C. After 12 h of reflux, the reaction batch was filtered in a 2 L flask and concentrated under vacuum (An identical batch was made under the same conditions, yield of both crude products was ca. 95%). Subsequently, the combined crude product was purified by shortpass-vacuum distillation at 27 mbar. The yield was 1105 g, which corresponded to 92% of the theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431710B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-0c82a5db2a7542659b61c211f2138390 |
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| Source note | uspto-grants-2013_04 |
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