Acetic Acid → Methyl 1H-imidazole-2-carboxylate
Reaction equation
C([N:20]1[CH:24]=[CH:23][N:22]=[C:21]1[C:25]([O:27][CH3:28])=[O:26])(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C(O)(=O)C>CO>[C:25]([C:21]1[NH:20][CH:24]=[CH:23][N:22]=1)([O:27][CH3:28])=[O:26]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
After a solution of 3.2 g (8.7 mmol.) of 1-trityl-2-carbomethoxyimidazole in 40 mL of a 5% solution of acetic acid in methanol was refluxed for 30 minutes, it was concentrated in vacuo. Recrystallization from ethanol afforded colorless needles, mp 187°-188° C.
Workup
- concentrationit was concentrated in vacuo
- customRecrystallization from ethanol afforded colorless needles, mp 187°-188° C.
Sources & evidence
- ORD record
- ord-3f70f74d51184acb8a75322580ecc016
- Source dataset
- uspto-grants-1991_08
- Patent number
- US05039691
Reaction notes
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