HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678868Generated: October 26, 2026
Potassium Hydroxide → 3-Cyano-4-carbamoyl-1,2,5-thiadiazole
https://huagongshe.com/reaction/1678868
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,2,5-Thiadiazole-3,4-dicarboxylic acid | HCID 270016 | — |
| Reactant | 1,2,5-Thiadiazole-3,4-dicarbonitrile | HCID 3825227 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Product | 3-Cyano-4-carbamoyl-1,2,5-thiadiazole | HCID 20364651 | — |
Reaction Steps
A method for preparing the monopotassium salt of 1,2,5-thiadiazol-3,4-dicarboxylic acid by double stage saponification of 3,4-dicyano-1,2,5-thiadiazole, this method comprising adding aqueous KOH to an aqueous suspension of 3,4-dicyano-1,2,5-thiadiazole in such amount that the molar ratio of 3,4-dicyano-1,2,5-thiadiazole to KOH is from about 1:1.01 to 1:0.8, and maintaining the temperature at from about 20° to 50° C. to thereby catalytically hydrogenate and form 3-cyano-4-carbamoyl-1,2,5-thiadiazole, effecting further hydrolysis by adding additional aqueous KOH in such amount as to result in an overall molar ratio of 3,4-dicyano-1,2,5-thiadiazole to KOH of from about 1:2.0 to 1:2.35 and an overall molar ratio of 3,4-dicyano-1,2,5-thiadiazole to H2O of from about 1:20 to 1:23, at a temperature of from about 85° to 100° C., to thereby form a solution of the dipotassium salt of 1,2,5-thiadaizole-3,4-dicarboxylic acid, and separating the monopotassium salt by acidifying, to a pH of from about 2 to 3, said solution of dipotassium salt of 1,2,5-thiadiazole-3,4-dicarboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04077966 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-051207d795884190a26647310b291370 |
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| Source note | uspto-grants-1978_03 |
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