HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 84955Erstellt: 24. Oktober 2026
tert-Butyl acrylate → (E)-tert-Butyl 3-(2-(2-ethoxy-2-oxoethyl)phenyl)acrylate
https://huagongshe.com/de/reaction/84955
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | tert-Butyl acrylate | HCID 15458 | — |
| Edukt | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Edukt | Ethyl 2-(2-bromophenyl)acetate | HCID 2780092 | — |
| Edukt | alpha-Cyclohexylcyclohexanemethanamine | HCID 10774245 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | (E)-tert-Butyl 3-(2-(2-ethoxy-2-oxoethyl)phenyl)acrylate | HCID 86647801 | — |
Reaktionsschritte
To a mixture of ethyl 2-(2-bromophenyl)acetate (0.97 g, 4 mmol), t-butyl acrylate (0.51 g, 4 mmol), tris(dibenzylideneacetone)dipalladium(0) (91 mg, 0.1 mmol), dicyclohexylmethylamine (0.98 g, 5 mmol) in dioxane (5 mL) was added tri-tert-butylphosphine (0.2 mL, 1 N in toluene, 0.2 mmol). The mixture was heated at 70° C. for 30 minutes under N2. Ethyl acetate was added, and the mixture was filtered through diatomaceous earth. The filtrate was concentrated and purified by silica gel column chromatography eluting with hexanes and ethyl acetate (10:1) to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 7.79 (m, 1H), 7.72 (d, J=15.6 Hz, 1H), 7.34 (m, 3H), 6.40 (d, J=15.7 Hz, 1H), 4.06 (q, J=7.2 Hz, 2H), 3.84 (s, 2H), 1.48 (s, 9H), and 1.17 (t, J=2 Hz, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08846951B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-02bb524d6400491e80253008d44c0ca7 |
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| Quellennotiz | uspto-grants-2014_09 |
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