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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385181Generated: October 30, 2026

Hydrochloric Acid → 2-hydroxy-4-isothiocyanatobenzoic acid

https://huagongshe.com/reaction/385181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant4-Aminosalicylic AcidHCID 4649—
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-hydroxy-4-isothiocyanatobenzoic acidHCID 34849264%

Reaction Steps

Carbon disulfide (0.26 mL, 4.4 mmol) was added to a mixture comprising 4-amino-2-hydroxybenzoic acid (0.23 g, 1.5 mmol), tetrahydrofuran (1.0 mL), water (1.0 mL) and triethylamine (0.51 mL, 3.6 mmol), followed by stirring at room temperature for 31 hours. To the obtained reaction mixture, a tetrahydrofuran (1.0 mL) solution of iodine (0.41 g, 1.6 mmol) was dropwise added over a period of 3 minutes at 0° C., followed by stirring at 0° C. for further 2.5 hours. Thereafter, 1M hydrochloric acid (1.5 mL) and sodium sulfite (38 mg, 0.30 mmol) were added and mixed. Then, ethyl acetate (6 mL) was added, and the organic layer was separated and concentrated under reduced pressure to dryness. To the obtained residue, ethyl acetate (6 mL), water (2 mL) and sodium hydrogencarbonate (13 mg, 0.15 mmol) were added, and the organic layer was washed twice with water (2 mL) and then concentrated under reduced pressure to dryness. To the obtained residue, chloroform (1 mL) and hexane (3 mL) were added and thoroughly mixed, and then, an insoluble matter was removed by filtration. The filtrate was concentrated under reduced pressure to dryness to obtain 4-isothiocyanato-2-hydroxybenzoic acid as a brown-colored solid (0.18 g, yield: 64%, HPLC purity: 86%, HPLC retention time: 4.6 min). LC-MS ES-194 (retention time: 4.4 min, condition 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367857B2
Source datasetuspto-grants-2013_02
ORD IDord-7c8c90f2729b40c588a672c5b5630bcf
Source noteuspto-grants-2013_02