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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604961Generated: October 26, 2026

Water → 3-[(Carboxyphenyl)sulfanyl]benzenecarboxylic acid

https://huagongshe.com/reaction/604961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Iodobenzoic acidHCID 12060—
ReactantSodium SulfideHCID 14804—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
Product3-[(Carboxyphenyl)sulfanyl]benzenecarboxylic acidHCID 1664100239.1%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910770B2
Source datasetuspto-grants-2011_03
ORD IDord-9ee6d3f05c37480ca18511a320497b1d
Source noteuspto-grants-2011_03