HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Phenyl(2,4,6-trifluorophenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 2,4,6-Trifluorobenzoyl chloride | HCID 144895 | — |
| Solvent | Water | HCID 962 | — |
| Product | Phenyl(2,4,6-trifluorophenyl)methanone | HCID 2777009 | — |
Reaction Steps
2,4,6-trifluorobenzoyl chloride (5.0 g), benzene (5 ml) and ferric chloride (1.39 g) were heated at 80° C. for 16 h, then allowed to cool to room temperature. The reaction mixture was diluted with water, extracted with ethyl acetate (×2) and the combined organic extracts washed with brine, dried (MgSO4) and evaporated under reduced pressure (5.80 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08148572B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-d737ebcb26e74a079cebfd6ae9304fdb |
| Source note | uspto-grants-2012_04 |