HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → (E)-4-bromo-3-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (E)-3-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl ester | HCID 67504254 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | (E)-4-bromo-3-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl ester | HCID 67504522 | 51.3% |
Reaction Steps
To a stirred mixture of (E)-3-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl ester (3.20 g, 0.012 mol) in carbon tetrachloride (20 mL) under a nitrogen atmosphere was added N-bromosuccinimide (3.26 g, 0.018 mol) and benzoyl peroxide (295 mg, 0.001 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-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl ester (2.10 g, 50%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741327B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-bb3f25397f944f85a7a90471a6a73096 |
| Source note | uspto-grants-2010_06 |