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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426718Generated: October 31, 2026

Hydrochloric Acid → HCID 178470042, compound

https://huagongshe.com/reaction/426718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl chloroformateHCID 10928—
ReactantEthyl diazoacetateHCID 12192—
ReactantSodium thiocyanateHCID 516871—
ReactantHCID 21183914HCID 21183914—
SolventAcetonitrileHCID 6342—
ProductHCID 178470042HCID 178470042—

Reaction Conditions

Temperature19 °C

Reaction Steps

5-Ethoxycarbonylamino-1,2,3-thiadiazole-4-carboxylic Acid. A suspension of sodium thiocyanate (24.30 g, 0.30 mole) in acetonitrile (120 ml), maintained at 19° C., was treated dropwise over 22 minutes with a solution of ethyl chloroformate (28.7 ml, 0.30 mole) in acetonitrile (25 ml). The resultant mixture was stirred for 25 minutes at 20° C. and then ethyl diazoacetate (31.5 ml, 0.30 mole) was added. After stirring for 24 hours, 6.0 N hydrochloric acid (300 ml) was added with cooling. Acetonitrile solvent was removed in vacuo and the residual aqueous suspension was extracted several times with ether. Combined ether extracts were washed with water, dried (Na2SO4) and evaporated to leave 51.0 g of ethyl 5-ethoxy-carbonylamino-1,2,3-thiadiazole-4-carboxylate. This ester was hydrolyzed by refluxing for 6 hours in a mixture of ethanol (80 ml) and aqueous 6 N hydrochloric acid (400 ml) to yield the title acid; m.p. 179°-180° dec. after crystallization from nitromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04171363
Source datasetuspto-grants-1979_10
ORD IDord-24ccf11bc1384bae925b860950e35aaf
Source noteuspto-grants-1979_10