HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → [2-(Bromomethyl)phenyl]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | o-Tolylacetic acid | HCID 69519 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | [2-(Bromomethyl)phenyl]acetic acid | HCID 12889260 | — |
Reaction Conditions
| Temperature | 2.5 °C |
|---|
Reaction Steps
To a solution of 97.0 g (0.646 mol) o-tolylacetic acid in 1.75 L carbon tetrachloride was added 115.0 g (0.646 mol) N-bromosuccinimide and 3.4 g (0.021 mol) 2,2′-azobisisobutyronitrile. The mixture was heated at reflux under a nitrogen atmosphere for 4 h. After the mixture was cooled to 0-5° C. for 30 min, the solids were removed by filtration and washed with a small portion of carbon tetrachloride. This solid was triturated with water (0.8 L), collected on a filter, and washed with 500 mL of water to give 2-bromomethylphenylacetic acid. The filtrate was concentrated to a volume of 150 ml, and the resulting slurry cooled to 0-5° C. for 30 min. A second batch of product was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06515011B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-32516d67db21493ca0b55eeba5422a1f |
| Source note | uspto-grants-2003_02 |