HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866758Generated: October 30, 2026
Hydrochloric Acid → HCID 21183914, compound
https://huagongshe.com/reaction/866758
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 21184064 | HCID 21184064 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21183914 | HCID 21183914 | — |
Reaction Steps
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-ethoxycarbonylamino-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04101548 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-0ce0b7d5e65245a39bf6010d45ce23d4 |
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| Source note | uspto-grants-1978_07 |
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