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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1,2,5-Thiadiazole-3,4-dicarboxylic acidHCID 270016—
Reactant1,2,5-Thiadiazole-3,4-dicarbonitrileHCID 3825227—
ReactantPotassiumHCID 5462222—
Product3-Cyano-4-carbamoyl-1,2,5-thiadiazoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04077966
Source datasetuspto-grants-1978_03
ORD IDord-051207d795884190a26647310b291370
Source noteuspto-grants-1978_03