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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065103Generated: October 25, 2026

Sulfuric Acid → HCID 178441961, compound

https://huagongshe.com/reaction/1065103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcetic AnhydrideHCID 7918—
Reactant3,3-Dimethyl-2-oxobutanenitrileHCID 94527—
ReactantThiocarbohydrazideHCID 2724189—
SolventHydrochloric AcidHCID 313—
ProductHCID 178441961HCID 17844196197.1%

Reaction Steps

First 25.6 g (0.25 mol) of acetic anhydride and then 27.8 g (0.25 mol) of pivaloyl cyanide were introduced, in each case at room temperature, into 49.0 g (0.5 mol) of concentrated sulphuric acid, which had been initially introduced into the reaction vessel. After subsequently stirring this reaction mixture for 0.5 hour, it was stirred into a solution of 26.6 g (0.25 mol) of thiocarbohydrazide in 300 ml of 1 N HCl at 20°-30° C. When the addition had ended, the mixture was subsequently stirred at 50°-55° C. for a further 1.5 hours; after cooling, the reaction product which had precipitated was filtered off, washed with 200 ml of water and dried. 48.6 g (97% of theory) of 4-amino-6-tert.-butyl-3-mercapto-1,2,4-triazin-5(4H)-one (V) were obtained as colorless crystals of melting point 212°-214° C.; content according to a determination by gas chromatography >99 %. No further purification operations were necessary for subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04328340
Source datasetuspto-grants-1982_05
ORD IDord-c49fc2677e874fb7b13f2a099cde28b2
Source noteuspto-grants-1982_05