Hydrochloric Acid → 1H-1,2,4-triazol-5-ylthiourea

HRID 569736Notes

Reaction equation

HRID 569736 reaction equation
[NH:1]1[C:5]([NH:6][C:7]([NH:9]C(=O)C2C=CC=CC=2)=[S:8])=[N:4][CH:3]=[N:2]1.[OH-].[Na+].Cl>>[NH:1]1[C:5]([NH:6][C:7]([NH2:9])=[S:8])=[N:4][CH:3]=[N:2]1

Participants

4

Procedure

N-(1,2,4-triazol-5-yl)-N'-benzoylthiourea (26.0 g, 0.105 mole), from Example 6, was added at once to approximately 100ml of a 10% sodium hydroxide solution which had been preheated to boiling, and the resultant mixture was refluxed for 45 minutes. The solution was then cooled and acidified to approximately pH 3 with the addition of concentrated hydrochloric acid to provide a white solid precipitate. The solid was filtered, washed with water and dried for about 16 hours in a vacuum oven at approximately 100° C. The resultant off-white solid was stirred with about 150 ml of diethyl ether and filtered, and this procedure was repeated. The solid thus obtained was dried in a vacuum oven at about 50° C. to yield 10.4 g (69%) of N-(1,2,4-triazol-5-yl)thiourea as an off-white solid. The structural assignment was confirmed by nuclear magnetic resonance spectral analysis.

Workup

  1. temperatureThe solution was then cooled
  2. customto provide a white solid precipitate
  3. filtrationThe solid was filtered
  4. washwashed with water
  5. customdried for about 16 hours in a vacuum oven at approximately 100° C
  6. filtrationfiltered
  7. customThe solid thus obtained
  8. customwas dried in a vacuum oven at about 50° C.

Sources & evidence

ORD record
ord-7d38ea67366249079f108a6c2c0bd9a7
Source dataset
uspto-grants-1988_03
Patent number
US04734413

Reaction notes

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