HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538640Generated: October 30, 2026
Phosphorus oxychloride → 2-(5-Amino-1,3,4-thiadiazol-2-yl)-2-methylpropanenitrile
https://huagongshe.com/reaction/538640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Reactant | 2-Cyano-2-methylpropanoic acid | HCID 11367091 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(5-Amino-1,3,4-thiadiazol-2-yl)-2-methylpropanenitrile | HCID 117650903 | 32.7% |
Reaction Steps
300 mg (3.29 mmol) of thiosemicarbazide and 370 mg (3.27 mmol) of 2-Cyano-2-methylpropanoic acid are dissolved in dioxane (10.0 mL) and heated to 90° C. 300 μL (3.29 mmol) of POCl3 are added dropwise. The reaction is stirred at 90° C. for 1 h, cooled to RT and diluted with 1 N aq. HCl and DCM. The aq. layer is separated, 4 N aq. NaOH is added to reach pH 8 and then extracted with DCM. Then combined organic layer is washed with brine and dried. The solvent is removed under reduced pressure to afford 180 mg of 2-(5-amino[1,3,4]thiadiazol-2-yl)-2-methyl-propionitrile. Yield: 32%; ESI-MS: 169 [M+H]+; HPLC (Rt): 0.24 min (method B)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865744B1 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-53f5f61f81694070a76c07d7f6535c2a |
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| Source note | uspto-grants-2014_10 |
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