Oxalic Acid → HCID 20471304, compound

HRID 1995652Notes

Reaction equation

HRID 1995652 reaction equation
[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].[CH3:7][C:8]1[CH:9]=[C:10]([CH:17]=[CH:18][C:19]=1[CH3:20])[CH2:11][N:12]1[CH:16]=[CH:15][N:14]=[CH:13]1>C(O)C>[C:1]([OH:6])(=[O:5])[C:2]([OH:4])=[O:3].[CH3:7][C:8]1[CH:9]=[C:10]([CH:17]=[CH:18][C:19]=1[CH3:20])[CH2:11][N:12]1[CH:16]=[CH:15][N:14]=[CH:13]1

Participants

4

Reactant 2

HCID 971Oxalic AcidHCID 130453671-[(3,4-Dimethylphenyl)methyl]-1H-imidazole

Product 1

HCID 20471304HCID 20471304, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent2×

Procedure

A hot solution of oxalic acid (0.225 g,0.0025 mol) in dry ethanol (10 ml) was added to a solution of 1-(3,4-dimethylbenzyl)imidazole (0.46 g,0.0025 mol) in hot ethanol (20 ml). After boiling for 0.25 h, the solution was evaporated to afford a white solid. Recrystallisation of the solid from ethanol/petroleum ether (b.p. 40°-60°) afforded 1-(3,4-dimethylbenzyl)imidazole hydrogen oxalate as a white solid, m.p. 92°-93°.

Workup

  1. customthe solution was evaporated
  2. customto afford a white solid
  3. customRecrystallisation of the solid from ethanol/petroleum ether (b.p. 40°-60°)

Sources & evidence

ORD record
ord-01feb0faac0d4b00ab18d1c54d371785
Source dataset
uspto-grants-1983_09
Patent number
US04405634

Reaction notes

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