Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isopropanol | HCID 3776 | — |
| Edukt | 2-Bromoethanol | HCID 10898 | — |
| Edukt | 4-Amino-1,2,4-triazole | HCID 11432 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | HCID 178475127 | HCID 178475127 | — |
Reaktionsschritte
5.000 grams, 59.4 mmoles of 4-amino-1,2,4-triazole was dissolved in 200 ml of fresh acetonitrile and stirred vigorously. 29.800 grams of 2-bromoethanol was added slowly to the solution by pipet. After the addition was complete, the reaction mixture was heated for 20 hours at 80° C., until thin layer chromatography revealed that all of the 4-amino-1,2,4-triazole had been consumed. The reaction mixture was then allowed to cool to room temperature and then was rotary evaporated down to leave a viscous oil. Hot isopropyl alcohol was added to the oil dissolving it. Storage of the resultant solution in a refrigerator resulting in a large crop of a viscous oil of 1-ethanol-4-amino-1,2,4-triazolium bromide, 9.9332 g, 47.5 mmoles. Melting point 0-5° C.; DSC onset 180° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745635B1 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-636d9b24fc2f447daf8cdd76a40f5893 |
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| Quellennotiz | uspto-grants-2010_06 |
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