HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2177312Erstellt: 26. Oktober 2026
Ethyl Acrylate → Ethyl (2E)-3-[4-hydroxy-2-(trifluoromethyl)phenyl]prop-2-enoate
https://huagongshe.com/reaction/2177312
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acrylate | HCID 8821 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 4-Bromo-3-(trifluoromethyl)phenol | HCID 22277307 | — |
| Katalysator | Palladium Chloride | HCID 24290 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Ethyl (2E)-3-[4-hydroxy-2-(trifluoromethyl)phenyl]prop-2-enoate | HCID 90442064 | — |
Reaktionsschritte
Into a 500-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 4-bromo-3-(trifluoromethyl)phenol (5 g, 20.75 mmol, 1.00 equiv), N,N-dimethylformamide (60 mL), ethyl prop-2-enoate (10.5 g, 104.88 mmol, 5.06 equiv), PdCl2 (370 mg, 2.09 mmol, 0.10 equiv), P(tolyl)3 (1.28 g, 4.21 mmol, 0.20 equiv), DIEA (16.25 g). The resulting solution was stirred for overnight at 90° C. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1/8). This resulted in 2.6 g (42%) of ethyl (2E)-3-[4-hydroxy-2-(trifluoromethyl)phenyl]prop-2-enoate as a light yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09067898B1 |
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| Quelldatensatz | uspto-grants-2015_06 |
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| ORD ID | ord-40226ac7e7a3447c9b9553d7579d2e6e |
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| Quellennotiz | uspto-grants-2015_06 |
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