HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504399Generated: October 30, 2026
Dimethylformamide → (E)-ethyl 3-(2-amino-5-bromophenyl)acrylate
https://huagongshe.com/reaction/1504399
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Bromo-2-iodoaniline | HCID 823934 | — |
| Solvent | Water | HCID 962 | — |
| Product | (E)-ethyl 3-(2-amino-5-bromophenyl)acrylate | HCID 86278419 | 55.8% |
Reaction Steps
To a microwave vial was added, 4-bromo-2-iodoaniline (1.70 g, 5.71 mmol), PdOAc2 (0.064 g, 0.285 mmol), sodium bicarbonate (1.198 g, 14.27 mmol), ethyl acrylate (0.651 ml, 5.99 mmol) and DMF (1.902 ml). The reaction was heated in microwave for 1 hour at 80° C. The reaction was cooled to room temperature, diluted with water and extracted with DCM (3×). The combined organics were washed with water and brine, dried over magnesium sulfate, filtered and concentrated. The resulting material was concentrated, dissolved in minimal DCM and purified via column chromatography (silica gel 40 g, gradient elution 0 to 50% EtOAc:Heptane) to afford 0.860 g of (E)-ethyl 3-(2-amino-5-bromophenyl)acrylate. m/z (ESI) 270.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212182B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-6ac906ec0f1e438aace2af5e4a584e1b |
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| Source note | uspto-grants-2015_12 |
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