Methanol → HCID 13423729, Verbindung
Reaktionsgleichung
[C:1]([C:4]1[CH:9]=[C:8]([C:10]([CH3:13])([CH3:12])[CH3:11])[CH:7]=[C:6]([S:14]([CH3:17])(=[O:16])=[O:15])[C:5]=1[OH:18])([OH:3])=[O:2].S(=O)(=O)(O)O.[CH3:24]O>>[CH3:24][O:2][C:1]([C:4]1[CH:9]=[C:8]([C:10]([CH3:13])([CH3:12])[CH3:11])[CH:7]=[C:6]([S:14]([CH3:17])(=[O:16])=[O:15])[C:5]=1[OH:18])=[O:3]Komponenten
4
Versuchsvorschrift
1.0 g (0.003 mol) of 2-carboxy-4-(1,1-dimethylethyl)-6-methylsulfonylphenol prepared in Example 3 is dissolved in 6 ml of methanol, and heated under reflux with 0.1 ml of concentrated sulfuric acid for 2 days. The mixture is poured onto ice-water, and this is extracted with ethyl acetate, the solvent is removed in vacuo and the residue is subjected to chromatography on silica gel using ethyl acetate/toluene 4:1 as the eluting agent.
Aufarbeitung
- temperatureheated
- additionThe mixture is poured onto ice-water
- extractionthis is extracted with ethyl acetate
- customthe solvent is removed in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-c15f472ec7f346ed9c3ce48356232004
- Quelldatensatz
- uspto-grants-1987_04
- Patentnummer
- US04661636
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