HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 556280Erstellt: 26. Oktober 2026
Triethylamine → 4-Formylcinnamic acid tert-butyl ester
https://huagongshe.com/reaction/556280
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | tert-Butyl acrylate | HCID 15458 | — |
| Edukt | 4-Bromobenzaldehyde | HCID 70741 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Katalysator | Triphenylphosphine | HCID 11776 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Formylcinnamic acid tert-butyl ester | HCID 54147604 | 70% |
Reaktionsschritte
A solution of 4-bromo benzaldehyde (2 g, 10.8 mmol) in DMF (50 ml) and triethylamine (3.4 ml, 27 mmol) was degassed flushing N2 for 30 min. PPh3 (141 mg, 0.54 mmol), Pd(OAc)2 (48.4 mg, 0.21 mmol), NaHCO3 (1.84 g, 21.6 mmol) and tert-butyl acrylate (1.58 ml, 10.8 mmol) were added and the resulting mixture was heated to reflux for 3 h. Additional Pd(OAc)2 (24 mg) was added and the mixture was heated to 100° C. for 1 h. The solution was diluted with H2O and extracted with Et2O. The organic layer was dried over Na2SO4 and the solvent was evaporated under vacuo to give the crude product that was triturated in isopropyl ether to give 1.6 g of 3-(4-formyl-phenyl)-acrylic acid tert-butyl ester.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08058273B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-4c0e5a8c3bc640fb8024f6cba150baa7 |
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| Quellennotiz | uspto-grants-2011_11 |
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