Nitric Acid → HCID 12573606, compound
Reaction equation
[Na+:1].[Na+].[C:3]1([S:13]([O-:16])(=[O:15])=[O:14])[CH:8]=[CH:7][CH:6]=[C:5]([S:9]([O-:12])(=[O:11])=[O:10])[CH:4]=1.S(=O)(=O)(O)O.[OH-].[Ca+2].[OH-].[N+:25]([O-])([OH:27])=[O:26]>>[Na+:1].[Na+:1].[N+:25]([C:7]1[CH:8]=[C:3]([S:13]([O-:16])(=[O:15])=[O:14])[CH:4]=[C:5]([S:9]([O-:12])(=[O:11])=[O:10])[CH:6]=1)([O-:27])=[O:26]Participants
Conditions
- Temperature
- 80 °C
Procedure
A 300 g amount of 1,3-benzenedisulfonic acid disodium salt is added to 400 ml of concentrated sulfuric acid in a 2 liter-three neck flask fitted with a stirrer, thermometer, condenser and a dropping funnel. The mixture is warmed to 80° C., then, without heating, 200 ml of fuming nitric acid is added dropwise maintaining the reaction temperature at 85°-89° C. When the acid addition is complete the reaction mixture is heated at 85°-88° C. for an additional 4 hours then is allowed to cool overnight. The mixture is poured slowly into ice-water and neutralized to pH 5-6 with calcium hydroxide. The precipitate formed is filtered off and the filtrate is basified to pH 10 with sodium carbonate. Again the precipitate formed is filtered off and the filtrate is concentrated to a small volume. The resulting residue is dissolved in boiling water and filtered. A total of 82 g of 5-nitrobenzene-1,3-disulfonic acid disodium salt is obtained by cooling the filtrate and collecting the precipitate.
Workup
- customfitted with a stirrer
- temperaturewithout heating
- temperaturemaintaining the reaction temperature at 85°-89° C
- additionWhen the acid addition
- temperatureis heated at 85°-88° C. for an additional 4 hours
- temperatureto cool overnight
- customThe precipitate formed
- filtrationis filtered off
- customAgain the precipitate formed
- filtrationis filtered off
- concentrationthe filtrate is concentrated to a small volume
- dissolutionThe resulting residue is dissolved
- filtrationfiltered
Sources & evidence
- ORD record
- ord-22c0efaef56f49f9a915ca11cbe32771
- Source dataset
- uspto-grants-1979_10
- Patent number
- US04172089
Reaction notes
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