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Hydrazinecarboxaldehyde → 3-(4-nitrophenyl)-1H-1,2,4-triazole

HRID 1807198
ノート
印刷プレビュー

反応式

HRID 1807198 の反応式
Cl.CO[C:4](=[NH:14])[C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][CH:6]=1.[CH:15]([NH:17][NH2:18])=O>N1C=CC=CC=1>[N+:11]([C:8]1[CH:7]=[CH:6][C:5]([C:4]2[NH:18][N:17]=[CH:15][N:14]=2)=[CH:10][CH:9]=1)([O-:13])=[O:12]
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 12229HydrazinecarboxaldehydeHCID 12410479HCID 12410479、化合物

生成物 1

HCID 28252243-(4-nitrophenyl)-1H-1,2,4-triazole

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

4-Nitro-benzimidic acid methyl ester hydrochloride (635 mg, 2.93 mmol) was suspended in pyridine (7 mL) and formic hydrazide (Aldrich, 178 mg, 2.95 mmol) was added and the mixture was stirred at rt for 1 hr. The solvent was removed and the residue was dissolved in toluene (10 mL) and the mixture was stirred at reflux for 1.5 hrs. the mixture was cooled and water was added. The organic layer was separated and dried over sodium sulfate. The solvent was removed and the residue was suspended in 25% EtOAc/Hexanes and the solid was filtered to give a solid. 510 mg.

後処理

このページの内容参加物実験手順後処理出典と根拠反応ノート
  1. customThe solvent was removed
  2. dissolutionthe residue was dissolved in toluene (10 mL)
  3. stirringthe mixture was stirred
  4. temperatureat reflux for 1.5 hrs
  5. temperaturethe mixture was cooled
  6. additionwater was added
  7. customThe organic layer was separated
  8. dry with materialdried over sodium sulfate
  9. customThe solvent was removed
  10. filtrationthe solid was filtered
  11. customto give a solid

出典と根拠

ORDレコード
ord-e9d962c9286948cbac36aa0a6d7abc96
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08354444B2

反応ノート

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