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Ethyl Bromide → HCID 178462842、化合物

HRID 20257
ノート
印刷プレビュー

反応式

HRID 20257 の反応式
[NH2:1][N:2]1[CH:6]=[N:5][N:4]=[CH:3]1.[CH2:7]([Br:9])[CH3:8]>C(#N)C>[Br-:9].[CH2:7]([N+:5]1[N:4]=[CH:3][N:2]([NH2:1])[CH:6]=1)[CH3:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6332Ethyl BromideHCID 114324-Amino-1,2,4-triazole2 回

生成物 1

HCID 178462842HCID 178462842、化合物

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒2 回

実験手順

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.

後処理

  1. customA 500 ml round bottom flask equipped with an overhead stirrer
  2. customhad been consumed
  3. customThe resultant solution was then rotary evaporated down
  4. customto leave a colorless oil which
  5. customslowly crystallized
  6. temperatureSolid material was heated to 60 C
  7. waitfor 5 hours under high vacuum
  8. customCrystalline 1-ethyl-4-amino-1,2,4-triazolium bromide was recovered in essentially quantitative yield and high purity, 22.94 g, 117 mmoles
  9. custom150° C.

出典と根拠

ORDレコード
ord-61caf7398085455b86789c48313e7871
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07745635B1

反応ノート

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