HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dichlorobenzoic acid → 3,4-Dichloro-2-methylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dichlorobenzoic acid | HCID 5817 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4-Dichloro-2-methylbenzoic acid | HCID 10584356 | — |
Reaction Steps
n-Butyl lithium (2.5M in hexanes, 180 ml) was added during 1 hour to a stirred solution of 3,4-dichlorobenzoic acid (40.0 g) at -78° C. and stirring maintained at that temperature overnight. A solution of methyl iodide (72 ml) in tetrahydrofuran was then added during 1.5 hours and the mixture kept at -78° C. for 3 hours and allowed to warm to room temperature overnight. The solvent was evaporated and the mixture added to water, acidified (concentrated hydrochloric acid) and extracted (ethyl acetate). The extract was dried (magnesium sulphate), evaporated and triturated (ether) to give 3,4-dichloro-2-methylbenzoic acid (33.3 g) as a white solid, m.p. 177°-178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05374606 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-dd024062847c4be5855e0e098498a274 |
| Source note | uspto-grants-1994_12 |