HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 225883Erstellt: 24. Oktober 2026
Ethyl Acrylate → Ethyl (E)-3-(6-amino-4-methylpyridin-3-yl)acrylate
https://huagongshe.com/de/reaction/225883
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acrylate | HCID 8821 | — |
| Edukt | Tri-o-tolylphosphine | HCID 80271 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Amino-5-bromo-4-methylpyridine | HCID 817695 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Propionitrile | HCID 7854 | — |
| Produkt | Ethyl (E)-3-(6-amino-4-methylpyridin-3-yl)acrylate | HCID 57440845 | 59% |
Reaktionsschritte
To a stirred solution of 2-amino-5-bromo-4-methylpyridine (10 g, 54 mmole) in propionitrile (50 mL) was added ethyl acrylate (17 mL, 157 mmole), DIEA (19 mL, 106 mmole), palladium(II) acetate (0.61 g, 2.7 mmole) and tri-o-tolylphosphine (1.64 g, 5.4 mmole). The reaction was purged with argon and heated at reflux for 6 hr, then was cooled to RT and concentrated to dryness under vacuum. The resulting residue was taken up in ethyl acetate and filtered through a pad of silica gel. The filtrate was concentrated and the remaining residue was triturated with 1:1 Et2O/petroleum ether (50 mL), filtered, and dried under vacuum to give the title compound (6.50 g, 59%) as a pale yellow solid: 1H NMR (400 MHz, DMSO-d6) δ 8.31 (s, 1 H), 7.66 (d, J=16.0 Hz, 1 H), 6.40 (br s, 2 H), 6.32 (d, J=16.0 Hz, 1 H), 6.28 (s, 1 H), 4.15 (q, 2 H), 2.24 (s, 3 H), 1.24 (t, 3 H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07557125B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-11ef8d546f2942e882ed85f1ac542b6a |
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| Quellennotiz | uspto-grants-2009_07 |
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