Reaktion #48535

Reaktionsgleichung

4-amino-1,2,4-triazole

Ethyl bromide

4-amino-1,2,4-triazole

→

1-ethyl-4-amino-1,2,4-triazolium bromide

Lösungsmittel

acetonitrile

acetonitrile

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeA 500 ml round bottom flask equipped with an overhead stirrer
2. 2
   Sonstigehad been consumed
3. 3
   SonstigeThe resultant solution was then rotary evaporated down
4. 4
   Sonstigeto leave a colorless oil which
5. 5
   Sonstigeslowly crystallized
6. 6
   TemperaturSolid material was heated to 60 C
7. 7
   workup.WAITfor 5 hours under high vacuum
8. 8
   SonstigeCrystalline 1-ethyl-4-amino-1,2,4-triazolium bromide was recovered in essentially quantitative yield and high purity, 22.94 g, 117 mmoles
9. 9
   Sonstige150° C.

Vorschrift

A 500 ml round bottom flask equipped with an overhead stirrer was charged with 10.00 grams of 4-amino-1,2,4-triazole and 200 ml of acetonitrile. Ethyl bromide, 45 ml, 65.0 grams, was added to the vigorously stirred acetonitrile reaction mixture. The reaction was stirred for 8 days at ambient temperature at which time, thin layer chromatography showed that all of the 4-amino-1,2,4-triazole had been consumed. The resultant solution was then rotary evaporated down to leave a colorless oil which slowly crystallized. Solid material was heated to 60 C. for 5 hours under high vacuum, whereupon it melted and lost the remaining solvent and resolidified. Crystalline 1-ethyl-4-amino-1,2,4-triazolium bromide was recovered in essentially quantitative yield and high purity, 22.94 g, 117 mmoles. Melting point: 63-67° C.; DSC onset: 150° C.

Quelle