HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250553Generated: October 26, 2026
Pyridine → Ethyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoate
https://huagongshe.com/reaction/2250553
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | Ethyl 3-oxo-4-phenylbutanoate | HCID 225855 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoate | HCID 57444525 | 67.5% |
Reaction Steps
To a suspension of magnesium chloride (1.46 g) in tetrahydrofuran (10 ml) was added a solution of ethyl 3-oxo-4-phenylbutanoate (2.0 g) in tetrahydrofuran (10 ml) and the mixture was cooled to 0° C., then pyridine (25 ml) was added. The mixture was stirred at 20° C. for 30 minutes, then a solution of 4-fluorobenzoyl chloride (2.44 g) in tetrahydrofuran (10 ml) was added at 0° C. After stirring at 20° C. for 2 hours, the mixture was partitioned between 0.5N hydrochloric acid and ethyl acetate. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:5) to give ethyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoate (2.15 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07317009B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-be610a8e787e4833816a4162aa604b4e |
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| Source note | uspto-grants-2008_01 |
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