Hydrochloric Acid → HCID 178526669, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:14]=[CH:15][C:16]=1[O:17]C)[CH2:7][N:8]1[CH:12]=[CH:11][N:10]=[C:9]1[SH:13])([O-:3])=[O:2].Cl>[OH-].[Na+]>[N+:1]([C:4]1[CH:5]=[C:6]([CH:14]=[CH:15][C:16]=1[OH:17])[CH2:7][N:8]1[CH:12]=[CH:11][N:10]=[C:9]1[SH:13])([O-:3])=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1-[3'-nitro-4'-methoxybenzyl]-2mercaptoimidazole (1.59 g, 6.0 moles) in 10% aqueous NaOH (200 ml) was refluxed for two hours, cooled, acidified with concentrated HCl, cooled and filtered. The crystalline product was washed with water. Recrystallization from ethanol provided 1.25 g (80%) of product as yellow prisms: mp 225-227° (dec).
Workup
- temperaturecooled
- temperaturecooled
- filtrationfiltered
- washThe crystalline product was washed with water
- customRecrystallization from ethanol
Sources & evidence
- ORD record
- ord-a1505d89cc864e6c983beac068d036b6
- Source dataset
- uspto-grants-1991_02
- Patent number
- US04992459
Reaction notes
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