HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654118Generated: November 3, 2026
Acetone → Ethyl 4-oxo-2-(2,2,2-trifluoroacetyl)pentanoate
https://huagongshe.com/reaction/1654118
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-oxo-2-(2,2,2-trifluoroacetyl)pentanoate | HCID 10933598 | — |
Reaction Steps
36.8 g of ethyl 4,4,4-trifluoroacetoacetate were mixed in 400 ml of tetrahydrofuran and 9.6 g of sodium hydride were added at 15° C. over 30 minutes. The mixture was stirred at 20° C. for 1 hour and 0.4 g of potassium iodide and 100 ml of acetone were added. 21 g of chloroacetone in 75 ml of tetrahydrofuran were added dropwise over 15 minutes and the mixture was refluxed for 96 hours and then distilled to obtain 24.4 g of the expected product with a boiling point of 65° C. (0.2 mbar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05405865 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-d1095c1ee73041f9955c22b7a888526d |
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| Source note | uspto-grants-1995_04 |
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