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Hydrochloric Acid → 4-methyl-5-phenyl-4H-1,2,4-triazole-3-thiol

HRID 257166
ノート
印刷プレビュー

反応式

HRID 257166 の反応式
[C:1]([NH:9][NH:10][C:11]([NH:13][CH3:14])=[S:12])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([O-])(O)=O.[Na+].Cl>>[CH3:14][N:13]1[C:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[N:9][NH:10][C:11]1=[S: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 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 27461131-Benzoyl-4-methyl-3-thiosemicarbazide

生成物 1

HCID 7197994-methyl-5-phenyl-4H-1,2,4-triazole-3-thiol

実験手順

A stirred mixture of 1-benzoyl-4-methylthiosemicarbazide (20.9 g, 1.00×10-1 mole) and 1 molar aqueous NaHCO3 (1000 ml, 1 mole) was heated to reflux. After refluxing overnight the reaction was cooled in an ice bath. With stirring the solution was carefully acidified by the dropwise addition of conc. HCl (92 ml, 1.1 mole). A colorless precipitate formed and this was subsequently collected by filtration. Crystallization from ethanol afforded colorless, chunky crystals, Mp 164°-166° C.

後処理

  1. temperaturewas heated to reflux
  2. temperatureAfter refluxing overnight the reaction
  3. temperaturewas cooled in an ice bath
  4. customA colorless precipitate formed
  5. filtrationthis was subsequently collected by filtration
  6. customCrystallization from ethanol afforded colorless

出典と根拠

ORDレコード
ord-92791f020f104e4283eafa221ee033dc
出典データセット
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05260450

反応ノート

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