HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604961Generated: October 26, 2026
Water → 3-[(Carboxyphenyl)sulfanyl]benzenecarboxylic acid
https://huagongshe.com/reaction/604961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Iodobenzoic acid | HCID 12060 | — |
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[(Carboxyphenyl)sulfanyl]benzenecarboxylic acid | HCID 16641002 | 39.1% |
Reaction Steps
To a solution of 3-iodobenzoic acid (24.8 g, 100.0 mmol) was dissolved in anhydrous DMF (100.0 mL) was added potassium carbonate (6.9 g, 50.0 mmol). The reaction mixture was heated to 100° C. for 5 minutes and sodium sulphide (4.3 g, 55.0 mmol) and copper iodide (1.9 g, 10.0 mmol) was added and the reaction mixture was heated to reflux under an atmosphere of nitrogen for 12 hours. Water (500.0 mL) was then added and the reaction mixture was heated to boiling with activated carbon. The carbon was filtered off while hot into an excess of 6N HCl (50.0 mL). A precipitate formed on cooling to room temperature and was collected by filtration and washed with water to afford (5.36 g, 19.5%) of the desired 3-[(carboxyphenyl)sulfanyl]benzenecarboxylic acid (GM71/7) as an off-white powder. M.S. m/z 272.73 (M−1)+. 1H NMR (300.13, d6-DMSO) 7.32-7.63 (4H, m, 4×ArH), 7.84-7.99 (4H, m, 4×ArH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07910770B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-9ee6d3f05c37480ca18511a320497b1d |
|---|
| Source note | uspto-grants-2011_03 |
|---|