HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(Bromomethyl)-5-(trifluoromethyl)furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methyl-5-(trifluoromethyl)furan | HCID 10953688 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(Bromomethyl)-5-(trifluoromethyl)furan | HCID 2794605 | 78.6% |
Reaction Steps
To a solution of 2-methyl-5-(trifluoromethyl)furan (4 g, 26.6 mmol) in chloroform (60 ml) were added N-bromosuccinimide (5.2 g, 29.3 mmol) and 2,2′-azobis(isobutyronitrile) (220 mg, 1.33 mmol). The reaction solution was heated under reflux for 15 min. The reaction solution was cooled, poured into water (200 ml) and was extracted with chloroform. The extract was washed with water and saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure to give 2-(bromomethyl)-5-(trifluoromethyl)furan (4.79 g, 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06982348B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-a54835f45fca449f8ff1660eda4ae0c1 |
| Source note | uspto-grants-2006_01 |