HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879280Generated: October 30, 2026
Triethylamine → Ethyl 4,4-difluoro-3-oxo-2-(piperidin-1-ylmethylidene)butyrate
https://huagongshe.com/reaction/1879280
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2-Difluoroacetyl fluoride | HCID 2778914 | — |
| Reactant | Ethyl 3-(piperidin-1-yl)prop-2-enoate | HCID 53394980 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 4,4-difluoro-3-oxo-2-(piperidin-1-ylmethylidene)butyrate | HCID 75152979 | 83.4% |
Reaction Steps
Ethyl 3-piperidin-1-ylacrylate (94%, 9.4 g, 48 mmol) was initially charged in toluene (100 ml) and cooled to −30° C. At this temperature, difluoroacetyl fluoride (5.0 g, 51 mmol) was introduced. Triethylamine (7.7 g, 77 mmol) was then added to the reaction mixture. The reaction mixture was stirred at −30° C. for 3 h and then, over a period of 1 h, warmed to room temperature. The reaction mixture was washed with deionized water (50 ml). After separation of the phases, the aqueous phase was extracted once with toluene (100 ml). The toluene phases were combined and washed with an aqueous saturated NaCl solution (100 ml), and the solvent was then removed under reduced pressure. This gave ethyl 4,4-difluoro-3-oxo-2-(1-piperidin-1-ylmethylidene)butyrate as an orange oil (amount: 12.3 g; purity according to GC: 85.4%; yield: 83.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314233B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-8c9aca29865a4d1cb21e0938ab5a08dc |
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| Source note | uspto-grants-2012_11 |
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