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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 385175Erstellt: 23. Oktober 2026

Hydrochloric Acid → 4-Isothiocyanatobenzoic acid

https://huagongshe.com/de/reaction/385175

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIodineHCID 807—
Edukt4-Aminobenzoic AcidHCID 978—
EduktCarbon DisulfideHCID 6348—
EduktTriethylamineHCID 8471—
EduktSodium SulfiteHCID 24437—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Isothiocyanatobenzoic acidHCID 242946100%

Reaktionsschritte

Carbon disulfide (0.66 mL, 11 mmol) was added to a mixture comprising 4-aminobenzoic acid (0.50 g, 3.6 mmol), tetrahydrofuran (2.5 mL), water (2.5 mL) and triethylamine (1.3 mL, 9.1 mmol), followed by stirring at room temperature for 24 hours. To the obtained reaction mixture, a tetrahydrofuran (2.5 mL) solution of iodine (1.0 g, 4.0 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 (3.6 mL) and sodium sulfite (91 mg, 0.72 mmol) were added and stirred. Then, ethyl acetate (15 mL) was added, and the organic layer was separated and concentrated under reduced pressure to dryness. To the residue, ethyl acetate (5 mL) and hexane (5 mL) were added and thoroughly mixed, and then, the insoluble matter was collected by filtration to obtain 4-isothiocyanatobenzoic acid as a colorless solid (0.65 g, yield: 100%, HPLC purity: 92%, HPLC retention time: 3.7 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-ab2b50207f4f43b9b58b852686443ab6
Quellennotizuspto-grants-2013_02