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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385178Generated: October 26, 2026

Hydrochloric Acid → 4-Isothiocyanato-2-chlorobenzoic acid

https://huagongshe.com/reaction/385178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
Reactant4-Amino-2-chlorobenzoic acidHCID 17154—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-Isothiocyanato-2-chlorobenzoic acidHCID 2273100662%

Reaction Steps

Carbon disulfide (0.26 mL, 4.4 mmol) was added to a mixture comprising 4-amino-2-chlorobenzoic acid (0.26 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 24.5 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 5 minutes at 0° C., followed by stirring at 0° C. for further two hours. Thereafter, 1M hydrochloric acid (1.5 mL) and sodium sulfite (38 mg, 0.30 mmol) were added and stirred. Then, ethyl acetate (6 mL) was added, and the organic layer was separated and concentrated under reduced pressure to dryness. To the residue, water (4 mL) and sodium hydrogencarbonate (0.14 g, 1.7 mmol) were added, and the insoluble matter was removed by filtration. To the filtrate, 1M hydrochloric acid (1.5 mL) and water (2.0 mL) were added, and the precipitated solid was collected by filtration. To this solid, ethyl acetate (6 mL), water (2.0 mL) and sodium hydrogencarbonate (25 mg, 1.7 mmol) were added, and the organic layer was concentrated under reduced pressure to dryness to obtain 4-isothiocyanato-2-chlorobenzoic acid as a white solid (0.20 g, yield: 62%, HPLC purity: 91%, HPLC retention time: 3.9 min). LC-MS ES-212, 214 (retention time: 4.2 min, condition 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367857B2
Source datasetuspto-grants-2013_02
ORD IDord-b03e4b7becd84cedbfd998405342dfd3
Source noteuspto-grants-2013_02