Acetic Acid → HCID 13019874, compound
Reaction equation
Cl.[CH2:2]([S:4][C:5]1[N:6]([C:10]2[CH:15]=[CH:14][C:13](C)=[CH:12][CH:11]=2)[CH:7]=[CH:8][N:9]=1)[CH3:3].Br.C(O)(=[O:20])C>>[CH2:2]([S:4][C:5]1[N:6]([C:10]2[CH:15]=[CH:14][C:13]([OH:20])=[CH:12][CH:11]=2)[CH:7]=[CH:8][N:9]=1)[CH3:3]Participants
4
Procedure
A mixture of 14 parts of 2-(ethylthio)-1-(4-methylphenyl)-1H-imidazole monohydrochloride and 113 parts of hydrobromic acid solution 48% in glacial acetic acid is stirred and refluxed for 3 hours. The reaction mixture is evaporated and the residue is dissolved in water. The solution is neutralized with sodium hydrogen carbonate. The precipitated product is filtered off and crystallized from 2-propanol, yielding 8.3 parts (72.5%) of 4-[2-(ethylthio)-1H-imidazol-1-yl]phenol; mp. 165.2° C.
Workup
- temperaturerefluxed for 3 hours
- customThe reaction mixture is evaporated
- dissolutionthe residue is dissolved in water
- filtrationThe precipitated product is filtered off
- customcrystallized from 2-propanol
Sources & evidence
- ORD record
- ord-4ed0ae6185744065afb302dc5cc5a6cc
- Source dataset
- uspto-grants-1981_01
- Patent number
- US04244964
Reaction notes
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