Hydrochloric Acid → HCID 178433555, compound
Reaction equation
[NH2:1][C:2](=[S:17])[NH:3][N:4]([C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][CH:9]=1)[C:5](=O)[CH3:6].Cl>[OH-].[Na+].O>[CH3:6][C:5]1[N:4]([C:8]2[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][CH:9]=2)[N:3]=[C:2]([SH:17])[N:1]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
40 Parts of acetic acid, 2-(aminothioxomethyl)-1-(4-nitrophenyl)hydrazide are dissolved in a mixture of 10 parts of sodium hydroxide and 400 parts of water and the solution is stirred for 30 minutes at room temperature. The reaction mixture is acidified with concentrated hydrochloric acid. The precipitated product is filtered off, washed with water and with 2-propanol and crystallized from 1,4-dioxane, yielding 22.4 parts of 5-methyl-1-(4-nitrophenyl)-1H-1,2,4-triazole-3-thiol; mp. 202.1° C.
Workup
- filtrationThe precipitated product is filtered off
- washwashed with water and with 2-propanol
- customcrystallized from 1,4-dioxane
Sources & evidence
- ORD record
- ord-8d5b195950a24b459bc29ff98b6aeb02
- Source dataset
- uspto-grants-1981_05
- Patent number
- US04267179
Reaction notes
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