2,6-Naphthalenedisulfonic acid → 2,7-Naphthalenedisulfonic acid
Reaction equation
[CH:1]1[C:10]2[C:5](=[CH:6][C:7](S(O)(=O)=O)=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[S:15]([OH:18])(=[O:17])=[O:16]>O>[CH:9]1[C:10]2[C:5](=[CH:4][CH:3]=[C:2]([S:15]([OH:18])(=[O:17])=[O:16])[CH:1]=2)[CH:6]=[CH:7][C:8]=1[S:15]([OH:18])(=[O:17])=[O:16]Participants
3
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 23 °C
Procedure
To 520 g of the disulfonation reaction mixture obtained in Example 4 was added 180 ml of water to adjust the sulfuric acid concentration to 45% by weight. The mixture was cooled to 23° C. and the precipitated crystal was recovered by filtration to obtain 60 g of 2,7-naphthalenedisulfonic acid having a purity of 97%.
Workup
- concentrationthe sulfuric acid concentration to 45% by weight
- filtrationthe precipitated crystal was recovered by filtration
Sources & evidence
- ORD record
- ord-8273d9625dc94fbcbc5b250aff8a7a41
- Source dataset
- uspto-grants-1982_04
- Patent number
- US04324742
Reaction notes
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