HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980102Generated: October 25, 2026
Ammonium Hydroxide → 5-(3-Methylpentan-3-yl)-1,3,4-thiadiazol-2-amine
https://huagongshe.com/reaction/980102
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-Ethyl-2-methylbutyric acid | HCID 29846 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(3-Methylpentan-3-yl)-1,3,4-thiadiazol-2-amine | HCID 13234263 | 91.9% |
Reaction Steps
A solution containing 13.0 g of 2-ethyl-2-methylbutyric acid and 9.1 g of thiosemicarbazide in 125 ml of dioxane was stirred and heated to 90° C. To the stirred reaction mixture was added dropwise over thirty minutes 15.3 g of phosphorus oxychloride. Following complete addition, the reaction mixture was heated at 90° C. for six hours. The mixture was then cooled to about 30° C. and added to 100 g of ice. The aqueous mixture was made alkaline by the addition of ammonium hydroxide, and the alkaline solution was extracted several times with ethyl acetate. The extracts were combined, washed with water, dried, and the solvent was removed by evaporation under reduced pressure to afford 17.0 g of 2-amino-5-(1-ethyl-1-methylpropyl)-1,3,4-thiadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04636243 |
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| Source dataset | uspto-grants-1987_01 |
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| ORD ID | ord-497bff36f61f4d2ba87e5065a737b80f |
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| Source note | uspto-grants-1987_01 |
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