HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465818Generated: October 30, 2026
P-Cresol → 2-(4-Methylphenoxy)benzoic acid
https://huagongshe.com/reaction/465818
Participants
| Role | Name | HCID | Charge |
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| Reactant | P-Cresol | HCID 2879 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Methylphenoxy)benzoic acid | HCID 578656 | 90.3% |
Reaction Steps
To a solution of 5.95 g of p-cresol and 7.83 g of 2-chlorobenzoic in 50 mL of dimethylformamide at 25° was added, in portions, 14.50 g of anhydrous potassium carbonate. The resulting mixture was heated to 80°, and 0.10 g of copper(I) iodide was added. The reaction mixture then was refluxed for 16 hours. While still hot the mixture was poured onto water-ice. The resulting suspension was filtered, and the filtrate was adjusted to pH 3.0 using aqueous hydrochloric acid. The precipitate was recovered by filtration. The crude solid was dissolved in an aqueous sodium hydroxide solution. This solution was acidified to pH 6.0 using hydrochloric acid, filtered, and then acidified to pH 3.0. Filtration provided 5.67 g of 2-(4-methylphenoxy)benzoic acid which was employed in the following reaction without further purification. NMR (200 MHz, CDCl3): δ8.15 (d of d, 1H); 7.42 (d of d of d, 1H); 7.23-7.12 (m, 3H); 6.97 (d, 2H); 6.80 (d, 1H); 2.37 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05153197 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-0d5c4e0a215843edb4fe1be1e711ede0 |
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| Source note | uspto-grants-1992_10 |
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