Reaktionsgleichung
[CH3:1][S:2]([C:5]1[CH:13]=[CH:12][C:8]([C:9]([OH:11])=[O:10])=[CH:7][CH:6]=1)(=[O:4])=[O:3].S(=O)(=O)(O)O.[CH3:19]O>>[CH3:1][S:2]([C:5]1[CH:13]=[CH:12][C:8]([C:9]([O:11][CH3:19])=[O:10])=[CH:7][CH:6]=1)(=[O:3])=[O:4]Komponenten
4
Versuchsvorschrift
250 ml of a desiccated methanol solution containing 50 g (0.25 mol) of p-methylsulfonylbenzoic acid and 10 ml of concentrated sulfuric acid was refluxed by heating for 8 hours. The reaction mixture was then cooled with ice and the crystals thus precipitated were collected by filtration and washed with methanol to obtain 48.2 g (0.225 mol) of the above described compound.
Aufarbeitung
- temperaturewas refluxed
- temperatureby heating for 8 hours
- temperatureThe reaction mixture was then cooled with ice
- customthe crystals thus precipitated
- filtrationwere collected by filtration
- washwashed with methanol
- customto obtain 48.2 g (0.225 mol) of the
Quellen und Nachweise
- ORD-Eintrag
- ord-f4eb3cf917914522b04af21b67219266
- Quelldatensatz
- uspto-grants-1986_09
- Patentnummer
- US04610957
Verknüpfte Notizen
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