HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893428Generated: October 29, 2026
Diethyl Carbonate → Ethyl 3-(4-Fluorophenyl)-3-Oxopropanoate
https://huagongshe.com/reaction/893428
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | 4'-Fluoroacetophenone | HCID 9828 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-(4-Fluorophenyl)-3-Oxopropanoate | HCID 2758844 | 78.4% |
Reaction Steps
To a suspension of sodium hydride (29.5 g of 60% oil dispersion, washed free of oil with hexane) in diethyl carbonate (88 mL, 0.726 mol) at room temperature under argon was added dropwise over 30 minutes p-fluoroacetophenone (50.0 g, 0.362 mol). Ethanol (0.1 mL) was added during the addition to initiate the reaction. After 2/3 of the ketone had been added, white solid had separated and Et2O (600 mL) was added to facilitate stirring. When the addition was complete the mixture was refluxed for 3 hours. The mixture was then placed in an ice bath, and the reaction was quenched by the dropwise addition of water (100 mL) and 5% KHSO4 solution (100 mL). The mixture was acidified with 10% H2SO4, the organic phase separated and washed with saturated NaHCO3 and saturated NaCl solutions, dried (MgSO4) and evaporated. The residue was distilled in vacuo to give title compound (59.66 g, 78%) as a colorless liquid, bp 115°-118° C. (1 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05124453 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-209097d361e44240943ac32e3a5a6d50 |
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| Source note | uspto-grants-1992_06 |
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