HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzoyl Peroxide → (E)-4-bromo-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzoyl Peroxide | HCID 7187 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | (E)-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester | HCID 66895334 | — |
| Lösungsmittel | Carbon Tetrachloride | HCID 5943 | — |
| Produkt | (E)-4-bromo-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester | HCID 66893744 | 31,6% |
Reaktionsschritte
To a stirred mixture of (E)-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester (5.80 g, 0.020 mol) in carbon tetrachloride (30 mL) under a nitrogen atmosphere was added N-bromosuccinimide (5.51 g, 0.031 mol) and benzoyl peroxide (500 mg, 0.002 mol). Nitrogen gas was bubbled through the mixture for 5 min, and the resulting mixture was heated to reflux for 4 h. The reaction mixture was then placed in the refrigerator overnight. The solids formed were removed by filtration and the filtrate concentrated in vacuo. The crude product obtained was purified using flash column chromatography (silica gel (100-200 mesh), ethyl acetate/hexanes) to afford (E)-4-bromo-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester (2.30 g, 31%) as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07741327B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-b7d634ae72814e9599086035e6f89c16 |
| Quellennotiz | uspto-grants-2010_06 |