HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 3-Bromo-4-methylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | P-Toluic Acid | HCID 7470 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-Bromo-4-methylbenzoic acid | HCID 82130 | — |
Reaction Steps
Briefly described, p-toluic acid 2 is refluxed with N-bromo-succinimide and benzoyl peroxide in dry benzene to give a bromo-p-toluic acid 3 which, upon reaction with nitric acid, is converted to 3-nitro-4-bromomethyl benzoic acid 4. This is believed to be a new compound and represents a parent compound in the synthesis forming the subject matter of this invention. At slightly higher temperatures, above -10° C., the corresponding dinitro derivative 4a predominates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04189605 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-b3d130a825f44ee5b7586cd9c2e21cf2 |
| Source note | uspto-grants-1980_02 |