HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Tolylacetic acid → 2-(3-(Bromomethyl)phenyl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Tolylacetic acid | HCID 12121 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(3-(Bromomethyl)phenyl)acetic acid | HCID 10376509 | 31% |
Reaction Steps
To a solution of 3-methylphenylacetic acid (125 g) in tetrachloro methane (1660 ml), N-bromosuccinimide (148 g) and 2,2′-azobisisobutyronitrile (AIBN; 1.37 g) were added. The mixture was refluxed with heating. After termination of reaction, the solution was cooled with ice. The white precipitate was filtered by glass-filter. The filtrate was washed by tetrachloro methane. The filtrate together with washing liquid was concentrated. The obtained residue was dissolved into ethyl acetate. Thereto, hexane was added. The mixture was crystallized to obtain the title compound (59 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06462081B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-48e55850629f48fba4cc1d5c56cfd73b |
| Source note | uspto-grants-2002_10 |