HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753091Generated: October 23, 2026
Diisopropylethylamine → Ethyl 3-(Trifluoromethyl)pyrazole-4-carboxylate
https://huagongshe.com/en/reaction/1753091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Hydrazinium chloride | HCID 115031 | — |
| Reactant | Ethyl ethoxymethylene-3-oxo-4,4,4-trifluorobutyrate | HCID 6185754 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-(Trifluoromethyl)pyrazole-4-carboxylate | HCID 596095 | — |
Reaction Steps
To a suspension of hydrazine hydrochloride (10 g, 147 mmol) in EtOH (500 mL), DIPEA (45.3 mL, 267 mmol) was added slowly at −20° C. and stirred for 10 minutes. Then 2-[1-ethoxy-meth-(E)-ylidene]-4,4,4-trifluoro-3-oxo-butyric acid ethyl ester (Preparation 96 Step 1, 32 g, 133.33 mmol) was added to above solution and the resulting mixture was stirred at room temperature for 16 hours. The reaction mixture was concentrated under reduced pressure and residue was partitioned between EtOAc (200 mL) and water (50 mL). The organic layer was washed with water (25 mL), dried (Na2SO4) and evaporated in vacuo. The crude material was purified by silica gel column chromatography eluting with Hexane:EtOAc 90:10 to afford the title compound as off white solid (43%, 13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09163021B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-18b821e71bac48ef9446089e8e737330 |
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| Source note | uspto-grants-2015_10 |
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