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Hydrogen Bromide → 1-(4-Bromo-3-methylphenyl)-1,2,4-triazole

HRID 2392679
ノート
印刷プレビュー

反応式

HRID 2392679 の反応式
[CH3:1][C:2]1[CH:8]=[C:7]([N:9]2[CH:13]=[N:12][CH:11]=[N:10]2)[CH:6]=[CH:5][C:3]=1N.N([O-])=O.[Na+].C(N)CN.[BrH:22]>[Cu]Br>[CH3:1][C:2]1[CH:8]=[C:7]([N:9]2[CH:13]=[N:12][CH:11]=[N:10]2)[CH:6]=[CH:5][C:3]=1[Br:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 260Hydrogen Bromide2 回HCID 3301EthylenediamineHCID 144502622-Methyl-4-[1,2,4]triazol-1-yl-phenylamineHCID 23668193Sodium Nitrite

生成物 1

HCID 189801161-(4-Bromo-3-methylphenyl)-1,2,4-triazole収率 73%

試薬・触媒・溶媒 1

HCID 24593copper(I) bromide
触媒

実験手順

2-Methyl-4-(1,2,4-triazol-1-yl)aniline (550 mg, 4.4 mmol) in 48% HBr (10 ml) at 5° C. was stirred while sodium nitrite (304 mg, 4.4 mmol) was added portionwise over 5 minutes. The brown sludge was left stirring for 15 minutes and then added portionwise over 5 minutes to a refluxing mixture of copper (I) bromide (631 mg, 4.4 mmol) in 48% HBr (2 ml). The mixture was then heated at reflux for 1 minute, allowed to cool slightly, and poured into 10% ethylene diamine solution (20 ml). The aqueous solution was extracted with ethyl acetate, dried (Na2SO4), and evaporated to dryness under reduced pressure. The resulting mixture was purified by column chromatography on silica eluting with n-pentane/ethyl acetate (4-10%) to afford the title compound as a white solid (0.769 mg, 73%).

後処理

  1. additionwas added portionwise over 5 minutes
  2. waitThe brown sludge was left
  3. temperatureThe mixture was then heated
  4. temperatureat reflux for 1 minute
  5. temperatureto cool slightly
  6. extractionThe aqueous solution was extracted with ethyl acetate
  7. dry with materialdried (Na2SO4)
  8. customevaporated to dryness under reduced pressure
  9. customThe resulting mixture was purified by column chromatography on silica eluting with n-pentane/ethyl acetate (4-10%)

出典と根拠

ORDレコード
ord-a5677e4aabd24c44935be7f7f70ea307
出典データセット
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05801170

反応ノート

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