Hydrochloric Acid → HCID 21525460, compound
Reaction equation
C([O:4][CH2:5][CH2:6][O:7][C:8]1[CH:9]=[N:10][C:11]([C:14]2[N:15]([CH3:22])[C:16]([N+:19]([O-:21])=[O:20])=[CH:17][N:18]=2)=[N:12][CH:13]=1)(=O)C.[ClH:23]>C(O)C>[ClH:23].[OH:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[N:12][C:11]([C:14]2[N:15]([CH3:22])[C:16]([N+:19]([O-:21])=[O:20])=[CH:17][N:18]=2)=[N:10][CH:9]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.2 g. of 5-(2-acetoxyethoxy)-2-(5-nitro-1-methyl-2-imidazolyl)-pyrimidine is refluxed in 5 ml. of ethanol with 2.5 ml. of concentrated hydrochloric acid. After concentration under vacuum, the residue is recrystallized from ethyl acetate; m.p. 158°-160° C.
Workup
- concentrationAfter concentration under vacuum
- customthe residue is recrystallized from ethyl acetate
Sources & evidence
- ORD record
- ord-39e6f0d7b7ed4e53b8a09ab28a893419
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03966732
Reaction notes
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