Reaktion #1914819
ord-cd186954ca404a55bd09c2108542bbe0
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturto reflux for 3 h
- 2Sonstigethe solvent was removed
- 3workup.ADDITIONmethanol 5 was added
- 4workup.STIRRINGthe mixture was stirred
- 5Filtrationfiltered
- 6Einengenthe filtrate was concentrated
- 7workup.ADDITIONThe remaining oil was solidified by addition of hexane and ethanol
- 8workup.STIRRINGby stirring
- 9FiltrationFinal filtration
- 10Sonstigedrying
- 11Sonstigeresulted in pure 4-(2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-ylmethoxy)-butane-1-sulphonic acid sodium salt
Vorschrift
(2,3-Dihydro-thieno[3,4-b][1,4]dioxin-2-yl)-methanol (6.9 g, 40 mmol) was dissolved into tetrahydrofuran (100 mL) and blanketed by nitrogen. NaH (1.76 g) was added and stirring was continued for 30 min. Then butanesultone (6.0 g) was added dropwise after which the reaction mixture was brought to reflux for 3 h. Then it was cooled to 25° C. again, the solvent was removed, methanol 5 was added, the mixture was stirred, filtered and the filtrate was concentrated. The remaining oil was solidified by addition of hexane and ethanol, followed by stirring. Final filtration and drying resulted in pure 4-(2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-ylmethoxy)-butane-1-sulphonic acid sodium salt as was demonstrated by NMR and mass spectroscopy.