Potassium Hydroxide → 5-Mesyl-o-anisic acid
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]([S:13]([CH3:16])(=[O:15])=[O:14])=[CH:9][C:4]=1[C:5]([O:7]C)=[O:6].[OH-].[K+]>>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]([S:13]([CH3:16])(=[O:15])=[O:14])=[CH:9][C:4]=1[C:5]([OH:7])=[O:6]Komponenten
3
Versuchsvorschrift
Combine methyl 2-methoxy-5-methylsulfonylbenzoate (2.24 g, 9.2 mmol) and a 1 M aqueous potassium hydroxide solution (10 mL, 10 mmol). Heat to reflux. After 2 hours, filter while still hot, cool in an ice bath, and acidify by dropwise addition of a 1 M aqueous hydrochloric acid solution (11 mL) to give a solid. Collect the solid by filtration, rinse with water, and dry to give the title compound.
Aufarbeitung
- temperatureHeat to reflux
- filtrationfilter while still hot,
- temperaturecool in an ice bath
- additionacidify by dropwise addition of a 1 M aqueous hydrochloric acid solution (11 mL)
- customto give a solid
- customCollect the solid
- filtrationby filtration
- washrinse with water
- customdry
Quellen und Nachweise
- ORD-Eintrag
- ord-51e6a8f6e2ec4f5b836d67b9f2ad5d02
- Quelldatensatz
- uspto-grants-2001_04
- Patentnummer
- US06211199B1
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