HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-(Bromomethyl)-4-(trifluoromethyl)furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methyl-4-(trifluoromethyl)furan | HCID 21819750 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(Bromomethyl)-4-(trifluoromethyl)furan | HCID 21819753 | 60.1% |
Reaction Steps
6 g of the product of Stage D were refluxed for 1 and a half hours in 50 ml of carbon tetrachloride in the presence of 7.2 g of N-bromosuccinimide and 0.3 g of azobisisobutyronitrile and the mixture was allowed to return to room temperature and was filtered. The solvent was evaporated and the residue was chromatographed on silica (eluent: 98/2 ether/isopropyl ether) to obtain 5.5 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405865 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-b3d89a00b8414e9d93c3bacac0ffbde1 |
| Source note | uspto-grants-1995_04 |