反应 #48535

ord-61caf7398085455b86789c48313e7871

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他A 500 ml round bottom flask equipped with an overhead stirrer
  2. 2
    其他had been consumed
  3. 3
    其他The resultant solution was then rotary evaporated down
  4. 4
    其他to leave a colorless oil which
  5. 5
    其他slowly crystallized
  6. 6
    温度Solid material was heated to 60 C
  7. 7
    workup.WAITfor 5 hours under high vacuum
  8. 8
    其他Crystalline 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
    其他150° C.

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07745635B1uspto-grants-2010_06