HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389698Generated: October 30, 2026
Ethyl 2-bromo-3-(4-methoxyphenyl)-3-oxopropanoate → HCID 59587379, compound
https://huagongshe.com/reaction/389698
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2-bromo-3-(4-methoxyphenyl)-3-oxopropanoate | HCID 13048360 | — |
| Reactant | Sodium 2,6-difluorobenzoate | HCID 23698872 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59587379 | HCID 59587379 | 96.7% |
Reaction Steps
A solution of ethyl 2-bromo-3-(4-methoxyphenyl)-3-oxopropanoate (0.090 g, 0.3 mmol) and sodium 2,6-difluorobenzoate (0.054 g, 0.30 mmol) in ethanol (2 mL) was heated at 120° C. in the microwave for 10 minutes. The reaction mixture was diluted with EtOAc (25 mL) and water (25 mL). The organic phase was washed with water and brine, dried over MgSO4 and the solvent evaporated in vacuo. The residue was purified by silica gel column chromatography using a gradient of 0-40% EtOAc in hexanes to afford 3-ethoxy-1-(4-methoxyphenyl)-1,3-dioxopropan-2-yl 2,6-difluorobenzoate (0.108 g, 0.29 mmol, 96%) as a clear film. 1H NMR (CDCl3) δ 1.27 (3H, t), 3.89 (3H, s), 4.30 (2H, m), 6.47 (1H, s), 6.97 (4H, m), 7.46 (1H, m), 8.06 (2H, d). LCMS (1) Rt: 2.26 min; m/z (ES+) 379.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378095B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-be4053e71b4a4939b2a17ea4c33a982b |
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| Source note | uspto-grants-2013_02 |
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