HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-Bromohexyl prop-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 6-Bromo-1-hexanol | HCID 77970 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 6-Bromohexyl prop-2-enoate | HCID 15153819 | 65.2% |
Reaction Steps
Into a reactor, 30 g of 6-bromo-1-hexanol, 18.4 g of triethylamine, and 500 ml of benzene were charged, to which a solution of 16.5 g of acryloyl chloride in 200 ml of benzene was added dropwise, while stirring and cooling with ice, and stirred for 3 hours to give a reaction solution. The reaction solution was washed with a 3N-HCl and then with water, dried over sodium sulfate anhydride, and thereafter the solvent was evaporated and the residue was purified by the silica gel column chromatography (eluent; toluene) to give 25.4 g (Y., 65.1%) of 6-bromohexyl acrylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05702642 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-8d1309d325ad4d4d99b83b24a5598950 |
| Source note | uspto-grants-1997_12 |