HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435893Generated: October 28, 2026
Formaldehyde → 2-Methyl-4-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)-1,2,4-triazolidin-3-one
https://huagongshe.com/reaction/435893
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Methyl-4-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)semicarbazide | HCID 21454604 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Methyl-4-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)-1,2,4-triazolidin-3-one | HCID 21454607 | — |
Reaction Steps
The 2-methyl-4-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)semicarbazide prepared in Example 2 was dissolved in methanol (100 ml) in a glass reaction flask equipped with a mechanical stirrer and thermometer. Aqueous formaldehyde (12 ml; 37% concentration) was then added to the flask with stirring. The reaction mixture warmed to a temperature of about 35° C. Sufficient aqueous potassium hydroxide was then added to adjust the pH of the reaction medium to from about 7 to 8. A solid precipitate was formed. The precipitate was then recovered by filtration, was recrystallized from an ethyl acetate-heptane mixture and was dried under vacuum to yield the desired product 2-methyl-4-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)-1,2,4-triazolidin-3-one having a melting point of 187° to 188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04007031 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-666b1faadd784c4fb744a503169abfc1 |
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| Source note | uspto-grants-1977_02 |
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