HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860413Generated: October 25, 2026
Hydrochloric Acid → Ethyl 7-(4-fluorobenzoyl)-8-oxononanoate
https://huagongshe.com/reaction/860413
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 6-bromohexanoate | HCID 117544 | — |
| Reactant | 1-(4-Fluoro-phenyl)-butane-1,3-dione | HCID 432655 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 7-(4-fluorobenzoyl)-8-oxononanoate | HCID 57444527 | — |
Reaction Steps
A mixture of 1-(4-fluorophenyl)butane-1,3-dione (1.0 g), potassium carbonate (3.84 g), and tetrabutylammonium bromide (90 mg) in toluene (20 ml) was refluxed for 3 hours, then ethyl 6-bromohexanoate (1.18 ml) was added. After stirring at 100° C. for 3 hours, the mixture was partitoned between ethyl acetate and 0.5N hydrochloric acid. 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 7-(4-fluorobenzoyl)-8-oxononanoate (983 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07153854B2 |
|---|
| Source dataset | uspto-grants-2006_12 |
|---|
| ORD ID | ord-1b492a1ead7a4f64b5ca605ce0ca112b |
|---|
| Source note | uspto-grants-2006_12 |
|---|