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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385177Generated: October 25, 2026

Hydrochloric Acid → Benzoic acid, 3-isothiocyanato-

https://huagongshe.com/reaction/385177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantCarbon DisulfideHCID 6348—
Reactant3-Aminobenzoic AcidHCID 7419—
ReactantTriethylamineHCID 8471—
ReactantSodium SulfiteHCID 24437—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductBenzoic acid, 3-isothiocyanato-HCID 7504696%

Reaction Steps

Carbon disulfide (0.26 mL, 4.4 mmol) was added to a mixture comprising 3-aminobenzoic acid (0.20 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 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 mixed. Then, ethyl acetate (6 mL) was added, and the organic layer was separated and concentrated under reduced pressure to dryness. To the residue, ethyl acetate (4 mL) and water (2 mL) were added, and the organic layer was concentrated under reduced pressure to dryness to obtain 3-isothiocyanatobenzoic acid as a cream-colored solid (0.25 g, yield: 96%, HPLC purity: 95%, HPLC retention time: 3.6 min). LC-MS ES-178 (retention time: 4.0 min, condition 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367857B2
Source datasetuspto-grants-2013_02
ORD IDord-b508ba08c944470eb23b513138902056
Source noteuspto-grants-2013_02