HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265096Generated: October 27, 2026
Tri-o-tolylphosphine → (E)-Ethyl 3-(4-amino-2,5-difluorophenyl)-2-butenoate
https://huagongshe.com/reaction/2265096
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Ethyl trans-crotonate | HCID 429065 | — |
| Reactant | 4-Bromo-2,5-difluoroaniline | HCID 2773285 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (E)-Ethyl 3-(4-amino-2,5-difluorophenyl)-2-butenoate | HCID 86644278 | 29% |
Reaction Steps
A mixture of 4-bromo-2,5-difluoroaniline (5.0 g), ethyl crotonate (4.98 ml), palladium acetate (54.0 mg), tris(2-methylphenyl)phosphine (442 mg), and triethylamine (33.4 ml) was stirred at 110° C. in a nitrogen atmosphere for 48 hours. The reaction mixture was filtered through Celite, and the filtrate was concentrated. The obtained residue was 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 column chromatography (5% ethyl acetate/n-hexane) to give Compound 10a (1.69 g, 29%) as a brown 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-674295b49cb84d9abb2f0ca170725b16 |
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| Source note | uspto-grants-2010_12 |
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