HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic Acid → 4-Chlorobenzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 2-Bromotoluene | HCID 7236 | — |
| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | 2-Methylbenzoic acid | HCID 8373 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 4-Chlorobenzoic Acid | HCID 6318 | 90% |
Reaction Steps
Gilman et al., J. Am. Chem. Soc. 1940, 62, 2327f. describes the synthesis of benzoic acid derivatives by lithiation of the corresponding aryl bromides and subsequent carboxylation. The preparation of 2-methyl-benzoic acid by reaction of o-bromotoluene with n-butyllithium and subsequent carboxylation with solid CO2 achieves a yield of 83.8%. The reaction of 4-chlorobromobenzene with n-butyllithium and CO2 gives 4-chlorobenzoic acid with a 90% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06573404B2 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-d649eec50117447db680506d50995efe |
| Source note | uspto-grants-2003_06 |