Hydroquinone → HCID 178524617, compound
Reaction equation
[C:1]1([CH:8]=[CH:7][C:5]([OH:6])=[CH:4][CH:3]=1)[OH:2].[C:9](=[O:12])([O-:11])[O-].[K+:13].[K+].[CH:15]([O-:17])=[O:16].[K+]>>[OH:2][C:1]1[CH:8]=[C:7]([C:15]([O-:17])=[O:16])[C:5]([OH:6])=[CH:4][C:3]=1[C:9]([O-:11])=[O:12].[K+:13].[K+:13]Participants
4
Conditions
- Temperature
- 200 °C
Procedure
Dipotassium 2,5-dihydroxyterephthalate was prepared in the known “Kolbe-Schmidt” type reaction from hydroquinone. Hydroquinone was mixed with potassium carbonate and potassium formate, the latter which acted as a solvent when molten. The mixture was heated to 200° C. with stirring to provide a homogeneous solution. Excess carbon dioxide was bubbled through the stirred solution for about 8 h. Excess carbon dioxide optionally may be recycled. The reaction mass was drowned in water, and filtered. When the drowned and stirred reaction mass was filtered, the sparingly soluble dipotassium 2,5-dihydroxyterephthalate was separated from water-soluble potassium formate and potassium carbonate.
Workup
- customto provide a homogeneous solution
- customExcess carbon dioxide was bubbled through the stirred solution for about 8 h
- filtrationfiltered
- stirringstirred
- customreaction mass
- filtrationwas filtered
- customthe sparingly soluble dipotassium 2,5-dihydroxyterephthalate was separated from water-soluble potassium formate and potassium carbonate
Sources & evidence
- ORD record
- ord-417c612c452247228745164ad85a4be2
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08115007B2
Reaction notes
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