HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231390Generated: October 25, 2026
Acetic Acid → 4-amino-6-(1-cyclopropylethyl)-5-oxo-3-thioxo-tetrahydro-1,2,4-(2H,4H)-triazine
https://huagongshe.com/reaction/231390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Decanol | HCID 8174 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thiocarbohydrazide | HCID 2724189 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-amino-6-(1-cyclopropylethyl)-5-oxo-3-thioxo-tetrahydro-1,2,4-(2H,4H)-triazine | HCID 20032346 | — |
Reaction Steps
882 g (4.14 mols) of 4-(cyclopropyl-methyl-methylene)-N-methylrhodanine (as an E/Z mixture) are introduced into a solution of 712 g (17.8 mols) of sodium hydroxide in 4.4 l of water. After the addition of 7 ml of alkylaryl polyglycol ether, the mixture is stirred at 70° C. until complete dissolution occurs (about 16 hours). 438 g (4.14 mols) of thiocarbohydrazide and 115 ml of 1-decanol are then added, the mixture is stirred for one hour at 70° C., and 1525 ml of acetic acid are rapidly added dropwise, causing the reaction product to precipitate. The mixture is stirred at 80° C. for a further 2 hours, allowed to cool to room temperature and the precipitate is filtered off with suction, washed several times with water and also with petroleum ether and dried at 70° C. 725 g (82.6% of theory) of the above compound of melting point 142°-143° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04846881 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-ed94ae41352b495ba92f8bf3ddc675ad |
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| Source note | uspto-grants-1989_07 |
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