HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 420104Erstellt: 26. Oktober 2026
Triethylamine → Ethyl [3,5-bis(trifluoromethyl)phenyl]-{4-(isopropoxy)-3-vinylphenyl}phosphinate
https://huagongshe.com/reaction/420104
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-Bromo-1-isopropoxy-2-vinylbenzene | HCID 12542425 | — |
| Edukt | HCID 178476784 | HCID 178476784 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Ethyl [3,5-bis(trifluoromethyl)phenyl]-{4-(isopropoxy)-3-vinylphenyl}phosphinate | HCID 86633213 | 2,8% |
Reaktionsschritte
To a degassed solution of ethyl 3,5-bis(trifluoromethyl)-phenylphosphinate (3.33 g, 15.24 mmol) and 4-bromo-1-isopropoxy-2-vinylbenzene (3.33 mg, 13.8 mmol) in DMF (25 mL) were added the triethylamine (3.85 mL, 27.6 mmol) and tris(dibenzylideneacetone)dipalladium (2.53 g, 2.76 mmol). The mixture was heated in an oil bath at 70° C. overnight. The volatiles were removed in vacuo and the mixture was purified by column chromatography with 20 to 70% ethyl acetate in petroleum ether to afford compound BA3 (185 mg) as an oil in 2.8% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08093379B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-24024c65b1e94f0a93be85b2d7eebb40 |
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| Quellennotiz | uspto-grants-2012_01 |
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