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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 385177Erstellt: 24. Oktober 2026

Hydrochloric Acid → Benzoic acid, 3-isothiocyanato-

https://huagongshe.com/de/reaction/385177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIodineHCID 807—
EduktCarbon DisulfideHCID 6348—
Edukt3-Aminobenzoic AcidHCID 7419—
EduktTriethylamineHCID 8471—
EduktSodium SulfiteHCID 24437—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktBenzoic acid, 3-isothiocyanato-HCID 7504696%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367857B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-b508ba08c944470eb23b513138902056
Quellennotizuspto-grants-2013_02