HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691530Generated: November 2, 2026
Ethyl Acrylate → ethyl(2E)-3-(4-amino-2-fluorophenyl)acrylate
https://huagongshe.com/reaction/1691530
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Bromo-3-fluoroaniline | HCID 821848 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl(2E)-3-(4-amino-2-fluorophenyl)acrylate | HCID 20536506 | 96% |
Reaction Steps
To a mixture of 4-bromo-3-fluoroaniline (13.3 g, 70.0 mmol), ethyl acrylate (9.48 mL, 87.5 mmol), tris(2-methylphenyl)phosphine (8.52 g, 28.0 mmol), N,N-diisopropylethylamine (50 mL) and N,N-dimethylformamide (50 mL) was added palladium(II) acetate (0.786 g, 3.50 mmol), and the mixture was stirred at 110° C. for 5 hr under an argon atmosphere. The reaction mixture was cooled, and the solvent was evaporated under reduced pressure. Water and ethyl acetate were added to the residue, and the insoluble material was filtered off through celite. The filtrate was separated into the aqueous layer and the organic layer. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=20:80-60:40) to give the title compound (14.0 g, yield 96%). A part thereof was recrystallized to give yellow prisms.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153694B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-cf911990dea34769a75ea450d45865bd |
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| Source note | uspto-grants-2012_04 |
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