Reaction equation
[S:1](=[O:5])(=[O:4])([OH:3])O.[C:6]1([C:12]2[C:13]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>O>[C:18]1([C:13]2[C:12]([C:6]3[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=3)=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:23]=[CH:22][C:21]([S:1]([OH:5])(=[O:4])=[O:3])([S:1]([OH:3])(=[O:5])=[O:4])[CH2:20][CH:19]=1Participants
4
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 140 °C
Procedure
880 g of concentrated sulfuric acid were heated to 110° C, and 270.5 g of terphenyl were added. The temperature was raised to 140° C and left on that level for 4 hours. After cooling down to 100° C, 800 ml of water were added dropwise, and the mixture was allowed to cool and then filtered with suction, giving a crude product which was used direct in the next stage. Purity (HPLC): 99.7%; yield: 565 g.
Workup
- temperatureAfter cooling down to 100° C
- temperatureto cool
- filtrationfiltered with suction
Sources & evidence
- ORD record
- ord-2042710a350c43b99826428d2aed046a
- Source dataset
- uspto-grants-1991_04
- Patent number
- US05008472
Linked notes
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