Carbon Dioxide → 5-Aminosalicylic Acid
Reaction equation
[NH:1]([C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][CH:6]=1)C(C)=O.[OH-].[K+].[C:14](=[O:16])=[O:15]>>[NH2:1][C:5]1[CH:6]=[C:7]([C:14]([OH:16])=[O:15])[C:8]([OH:11])=[CH:9][CH:10]=1Participants
4
Conditions
- Temperature
- 185 °C
Procedure
p-Acetaminophenol 15 g, and potassium hydroxide 60 g were added into a 500 ml autoclave, and CO2 was introduced to perform a carboxylation reaction under a reaction pressure of 2.0 MPa and heated to 185° C., maintained for 14 hours, then the reaction was terminated, cooled to 80° C., and 1500 ml distilled water was added to dissolve potassium 5-aminosalicylate. After decolorization, the aqueous phase was acidified with 20˜30% hydrochloric acid until pH=4, cooled and then filtered to obtain the product of 5-aminosalicylic acid, the yield is 30%.
Workup
- additionwas introduced
- customa carboxylation reaction
- customunder a reaction pressure of 2.0 MPa
- temperaturemaintained for 14 hours
- customthe reaction was terminated
- temperaturecooled to 80° C.
- distillation1500 ml distilled water
- additionwas added
- dissolutionto dissolve potassium 5-aminosalicylate
- temperaturecooled
- filtrationfiltered
Sources & evidence
- ORD record
- ord-1613a4409bf749aba922a530acb89f4b
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067867B2
Reaction notes
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