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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197688Generated: October 30, 2026

3-Aminobenzoic Acid → 3-(4-Oxo-2-sulfanylidene-1,3-thiazolidin-3-yl)benzoic acid

https://huagongshe.com/reaction/2197688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminobenzoic AcidHCID 7419—
ReactantSodium HydroxideHCID 14798—
Reactant3,5-Dithia-4-thioxo-1,7-heptanedioic acidHCID 80618—
Product3-(4-Oxo-2-sulfanylidene-1,3-thiazolidin-3-yl)benzoic acidHCID 30288982.1%

Reaction Steps

3-amino-benzoic acid (6.00 g, 43.77 mmol), bis(carboxymethyl)trithiocarbonate (10.2 g, 45.09 mmol) in 1.029 N aqueous sodium hydroxide (44.5 g, 44.06 mmol) was heated at 100° C. for 16 h. The reaction mixture was cooled to room temperature. The precipitated solid was filtered, washed successively with 3N aqueous HCl (3×20 mL), water (3×20 mL), ethanol (2×20 mL) and dried in vacuum oven at 60° C. for 2 h to obtain 3-(4-oxo-2-thioxo-thiazolidin-3-yl)-benzoic acid (9.10 g, 82%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 4.34 (2H, s), 7.52-7.55 (1H, m), 7.67 (1H, t, J=8 Hz), 7.87 (1H, t, J=2 Hz), 8.02-8.05 (1H, dt, J=1.2 & 2.8 Hz); ESI-MS: 253.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338465B2
Source datasetuspto-grants-2012_12
ORD IDord-667f1617873d4482843988e4e999fbaa
Source noteuspto-grants-2012_12