HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenacyl bromide → 2,4-Dibromobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | 1-Bromo-3-fluorobenzene | HCID 14082 | — |
| Reactant | 2-Bromo-1-(4-fluorophenyl)ethan-1-one | HCID 96749 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 2-Bromo-4-fluorobenzoic acid | HCID 1268169 | — |
| Product | 2,4-Dibromobenzoic acid | HCID 11896 | — |
Reaction Steps
Some of the compounds of the general formula II are known and may be prepared by known methods. For example, 2-bromo-4-fluorobenzoic acid may be obtained from 1-bromo-3-fluorobenzene by acetylation and oxidation of the 2-bromo-4-fluoroacetophenone which is produced (Recl. Trav. Chim. Pays-Bas, 83 p. 1142, 1146 (1964)). The oxidation of 2,4-dibromoacetophenone using potassium permanganate to give 2,4-dibromobenzoic acid is described in J. Karnatak Univ. 1 p. 36 (1956). According to J. Chem. Soc. 85, 1267 ff. (1904), 5-chloro-2-bromobenzoic acid may be obtained by nitric acid oxidation of 5-chloro-2-bromotoluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05744638 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-59daf23e31604584b56f795e87da781f |
| Source note | uspto-grants-1998_04 |