HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → Diethyl [(1E)-3-bromoprop-1-en-1-yl]phosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Diethyl (1E)-prop-1-en-1-ylphosphonate | HCID 5702572 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Diethyl [(1E)-3-bromoprop-1-en-1-yl]phosphonate | HCID 5702525 | 58.5% |
Reaction Steps
To a solution of diethyl trans-1-propenylphosphonate (32.04 g.) in carbon tetrachloride (320 ml.) were added N-bromosuccinimide (41.65 g.) and dibenzoylperoxide (2.8 g.). The reaction mixture was heated to reflux for 1.5 hours and stirred for 30 minutes under ice-cooling. Insoluble materials were removed off by filtration and the filtrate was concentrated under reduced pressure to give an oily residue (63.09 g.), which was subjected to a column chromatography on silicagel and eluted with chloroform. The eluates were evaporated to dryness under reduced pressure to give an oily diethyl 3-bromo-trans-1-propenylphosphonate (27.04 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04206156 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-20ce39297641490bbb96e6488c05935b |
| Source note | uspto-grants-1980_06 |