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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2253559Erstellt: 26. Oktober 2026

Hydrochloric Acid → HCID 178468779, Verbindung

https://huagongshe.com/reaction/2253559

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBenzocaineHCID 2337—
EduktHydrazineHCID 9321—
EduktThiophosgeneHCID 10040—
EduktEthyl 4-isothiocyanatobenzoateHCID 71003—
Edukt4-EthoxycarbonylphenylthiosemicarbazideHCID 19745752—
EduktSodium NitriteHCID 23668193—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
ProduktHCID 178468779HCID 17846877990%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

0.1 Mol of ethyl p-aminobenzoate was mixed with 150 ml of water and stirred for 15 minutes. Thiophosgene (10 g) in 50 ml chloroform was added dropwise. The mixture was stirred for 2 hours at 15° C. The organic solution was washed with HCl 2N, dried and the solvent was removed under vacuum to obtain a yellow-red oil, that was used as crude product. 0.02 mMole of the obtained 4-ethoxycarbonylphenylisothiocyanate and 30 ml ethanol were stirred in a flask and added dropwise with 2 ml 85% hydrazine in 2 ml water. After 15 minutes the crude product separated and was filtered under vacuum. Yield 90%. 0.01 Mole of the obtained 4-ethoxycarbonylphenylthiosemicarbazide was mixed with a solution of 1.5 ml HCl 37% and 35 ml water. The mixture was cooled to 5° C. and 0.8 g sodium nitrite dissolved in 5 ml water was added dropwise. The mixture was stirred for 30 minutes at 5° C. The crude product was filtered, washed with water and dried. Yield 80%. The product was crystallized from methanol. The structure was confirmed by IR and NMR spectroscopy.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05232826
Quelldatensatzuspto-grants-1993_08
ORD IDord-6bb0f49f7b484b7d9fc48c25f6532664
Quellennotizuspto-grants-1993_08