HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771833Generated: November 1, 2026
Dimethylformamide → 2,3-Dimethyl-5-phenyl-benzoic acid
https://huagongshe.com/reaction/1771833
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 5-Bromo-2,3-dimethylbenzoic acid | HCID 66895989 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,3-Dimethyl-5-phenyl-benzoic acid | HCID 89444110 | 46.4% |
Reaction Steps
To a solution of 5-bromo-2,3-dimethyl-benzoic acid (690 mg, 3.0 mmol, 1.0 eq), phenylboronic acid (404 mg, 3.3 mmol, 1.1 eq) and Na2CO3 (958 mg, 9.0 mmol, 3.0 eq) in a mixture of EtOH (5 mL), DMF (20 mL) and water (5 mL) was added Pd(PPh3)4 (0.17 g, 0.15 mmol, 0.05 eq). The reaction was heated at 100° C. overnight then diluted with EtOAc and filtered through celite. The aqueous layer was acidified to pH 4-5 with diluted HCl and extracted with EtOAc. The combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue obtained was purified by column chromatography (petroleum ether:EtOAc, 10:1 then CH2Cl2:MeOH, 400:0 to 20:1) to give the title compound as a white solid (315 mg, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09249085B2 |
|---|
| Source dataset | uspto-grants-2016_02 |
|---|
| ORD ID | ord-b3bc182074c74af0adeae3d3b6888f4f |
|---|
| Source note | uspto-grants-2016_02 |
|---|