HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265085Generated: October 27, 2026
Ethyl Acrylate → Ethyl 3-(4-amino-2-fluorophenyl)prop-2-enoate
https://huagongshe.com/reaction/2265085
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 4-Bromo-3-fluoroaniline | HCID 821848 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | Ethyl 3-(4-amino-2-fluorophenyl)prop-2-enoate | HCID 53987187 | 76% |
Reaction Steps
4-Bromo-3-fluoroaniline (5.0 g) was dissolved in a mixed solvent of DMF (18 ml) and N,N-diisopropylethylamine (18 ml). Ethyl acrylate (3.9 ml), palladium acetate (295 mg), and tris(2-methylphenyl) phosphine (3.2 g) were added to the obtained mixture in a nitrogen atmosphere, and the mixture was stirred at 110° C. for 5 hours. The reaction mixture was filtered through Celite and separated with ethyl acetate and water. The organic layer was washed with a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by neutral silica gel column chromatography (14-25% ethyl acetate/n-hexane). The purified material was crystallized with n-hexane to obtain Compound 2a (4.2 g, 76%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855300B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-988024a7cabc462ca6d8a5bc74051e8d |
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| Source note | uspto-grants-2010_12 |
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