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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253559Generated: October 26, 2026

Hydrochloric Acid → HCID 178468779, compound

https://huagongshe.com/reaction/2253559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzocaineHCID 2337—
ReactantHydrazineHCID 9321—
ReactantThiophosgeneHCID 10040—
ReactantEthyl 4-isothiocyanatobenzoateHCID 71003—
Reactant4-EthoxycarbonylphenylthiosemicarbazideHCID 19745752—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 178468779HCID 17846877990%

Reaction Conditions

Temperature5 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05232826
Source datasetuspto-grants-1993_08
ORD IDord-6bb0f49f7b484b7d9fc48c25f6532664
Source noteuspto-grants-1993_08