HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2414402Erstellt: 25. Oktober 2026
Triethylamine → Ethyl 3-[2-(2-(t-butoxycarbonylamino)ethoxy)-4-cyanophenyl]acrylate
https://huagongshe.com/reaction/2414402
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl Acrylate | HCID 8821 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | t-Butyl [2-(5-cyano-2-iodophenoxy)ethyl]carbamate | HCID 11111864 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Ethyl 3-[2-(2-(t-butoxycarbonylamino)ethoxy)-4-cyanophenyl]acrylate | HCID 69921285 | — |
Reaktionsschritte
11.0 g (28.4 mmol) of 3-[2-(t-butoxycarbonylamino)ethoxy]-4-iodobenzonitrile was dissolved in 200 ml of DMF. 15.4 ml (142 mmol) of ethyl acrylate, 20 ml (142 mmol) of triethylamine and 127 mg (0.567 mmol) of palladium acetate were added to the obtained solution. They were stirred at 100° C. overnight and then treated with ethyl acetate as the extraction solvent in an ordinary manner to obtain the crude product. After the purification by the silica gel column chromatography, the title compound was obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06812231B2 |
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| Quelldatensatz | uspto-grants-2004_11 |
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| ORD ID | ord-6fcd5222fd0b47fe8a222238ed191871 |
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| Quellennotiz | uspto-grants-2004_11 |
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