HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508661Generated: October 29, 2026
Ethyl Acrylate → (E)-ethyl 3-(5-bromopyrazin-2-yl)acrylate
https://huagongshe.com/reaction/508661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 2,5-dibromopyrazine | HCID 11470421 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | (E)-ethyl 3-(5-bromopyrazin-2-yl)acrylate | HCID 53259408 | 8.6% |
Reaction Steps
A solution of 2,5-dibromopyrazine (238.0 mg, 1.0 mmol), ethyl acrylate (174.0 μL, 1.6 mmol), palladium(II) acetate (3.4 mg, 0.015 mmol), and tri(o-tolyl)phosphine (36.5 mg, 0.12 mmol) in DMF (1.4 mL) and diisopropylethylamine (0.7 mL) was heated at reflux (115° C. oil bath) for 4.4 h, cooled to room temperature, and then quenched with H2O. The suspension was extracted with EtOAc (300 mL). The extract was washed (brine) and dried. After solvent removal at reduced pressure, the residue was purified on silica gel (11% EtOAc/hexane) to give 22 mg (8.5%) of ethyl(E)-3-(5-bromo-2-pyrazinyl)-2-propenoate as a cream solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096544B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-f54a490d4cb44016b7176c0e9685e28d |
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| Source note | uspto-grants-2015_08 |
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