Oxalic Acid → HCID 20277167, compound
Reaction equation
[CH3:1][C:2]1([CH3:16])[CH:7]2[CH2:8][CH:3]1[CH2:4][CH2:5][CH:6]2[CH2:9][CH2:10][N:11]1[CH:15]=[CH:14][N:13]=[CH:12]1.[C:17]([OH:22])(=[O:21])[C:18]([OH:20])=[O:19]>C(O)C>[C:17]([OH:22])(=[O:21])[C:18]([OH:20])=[O:19].[CH3:1][C:2]1([CH3:16])[CH:7]2[CH2:8][CH:3]1[CH2:4][CH2:5][CH:6]2[CH2:9][CH2:10][N:11]1[CH:15]=[CH:14][N:13]=[CH:12]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1-[2-(6,6-dimethylbicyclo[3.1.1]heptan-2-yl)ethyl]imidazole (0.8 g, 3.67 mmol) hot ethanol (10 ml) was added to a solution of oxalic acid (0.3 g, 3.33 mmol) in hot ethanol (20 ml). After boiling the reaction mixture for 0.15 h, the solution was concentrated under reduced pressure to afford a white solid. Recrystallisation of the solid from propan-2-ol gave 1-[2-(6,6-dimethylbicyclo[3.1.1]heptan-2-yl)ethyl]imidazole hydrogen oxalate, m.p. 172°-174°.
Workup
- customfor 0.15 h
- concentrationthe solution was concentrated under reduced pressure
- customto afford a white solid
- customRecrystallisation of the solid from propan-2-ol
Sources & evidence
- ORD record
- ord-f18bbabb9b0c436383e733e2a30d6d93
- Source dataset
- uspto-grants-1985_06
- Patent number
- US04525475
Reaction notes
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