HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904593Generated: October 31, 2026
Hydrochloric Acid → Ethyl 3-(4-bromo-2,3,5,6-tetrafluorophenyl)-3-oxopropanoate
https://huagongshe.com/reaction/1904593
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Bromo-2,3,5,6-tetrafluorobenzoyl chloride | HCID 2783245 | — |
| Reactant | Propanedioic acid, monoethyl ester | HCID 3595298 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | 2,2'-Bipyridine | HCID 1474 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-(4-bromo-2,3,5,6-tetrafluorophenyl)-3-oxopropanoate | HCID 9974705 | 86.9% |
Reaction Steps
n-Butyllithium (192 ml, 2.4M in hexane) was slowly added to a stirred solution of 30.24 g monoethylmalonate and 15 mg 2,2'-bipyridine in 500 ml tetrahydrofuran cooled to -60° to -70° C. under nitrogen. After about half of the butyllithium had been added, the temperature of the mixture was raised to -20° to -25° C. at which temperature the remainder of the butyllithium was added. The reaction mixture was then recooled to -60° to -70° C. and 33.41 g 4-bromo-2,3,5,6-tetrafluorobenzoyl chloride in 10 ml tetrahydrofuran was added. The reaction mixture was allowed to warm to room temperature, stirred overnight, and then poured into 460 ml 1M hydrochloric acid. The organic layer was separated, dried (magnesium sulfate) and concentrated. The residue was dissolved in ether, washed with aqueous potassium bicarbonate solution, dried (magnesium sulfate), concentrated and distilled to give 34.18 g ethyl 4-bromo-2,3,5,6-tetrafluorobenzoylacetate, b.p. 112°-117° C.(0.8 mm.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04839355 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-d5d67c1bf99f4aa39c3bf2d2d717f6a3 |
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| Source note | uspto-grants-1989_06 |
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