Sodium Hydroxide → 4-Hydroxyphenylsulfonic acid disodium salt
Reaction equation
O.O.[Na+:3].[OH:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([O-:14])(=[O:13])=[O:12])=[CH:7][CH:6]=1.[OH-].[Na+]>C1(C)C=CC=CC=1>[Na+:3].[Na+:3].[OH:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([O-:14])(=[O:12])=[O:13])=[CH:7][CH:6]=1.[OH:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([O-:14])(=[O:12])=[O:13])=[CH:7][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 4-hydroxybenzenesulfonic acid sodium salt dihydrate (20 g, 86 mmol) in 1N aqueous sodium hydroxide (86 mL, 86 mmol) is stirred and heated at 50–60° C. for 1 hour. The solution is concentrated in vacuo at 50° C. to give a solid. The solid is suspended in anhydrous toluene and concentrated in vacuo. This process is repeated twice. The solid is dried at 50° C. at high vacuum for 18 hours to give 21.34 g of 4-hydroxybenzenesulfonic acid disodium salt.
Workup
- temperatureheated at 50–60° C. for 1 hour
- concentrationThe solution is concentrated in vacuo at 50° C.
- customto give a solid
- concentrationconcentrated in vacuo
- customThe solid is dried at 50° C. at high vacuum for 18 hours
Sources & evidence
- ORD record
- ord-bfa9679dccda4c6384a65e667bc80767
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07183304B2
Reaction notes
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