Nitrogen → Sodium 4-((2,3-dihydrothieno(3,4-b)(1,4)dioxin-2-yl)methoxy)butane-1-sulfonate
Reaktionsgleichung
[O:1]1[CH:6]([CH2:7][OH:8])[CH2:5][O:4][C:3]2=[CH:9][S:10][CH:11]=[C:2]12.N#N.[H-].[Na+:15].[CH2:16]1[S:21](=[O:23])(=[O:22])[O:20][CH2:19][CH2:18][CH2:17]1>O1CCCC1>[Na+:15].[O:1]1[CH:6]([CH2:7][O:8][CH2:19][CH2:18][CH2:17][CH2:16][S:21]([O-:23])(=[O:22])=[O:20])[CH2:5][O:4][C:3]2=[CH:9][S:10][CH:11]=[C:2]12Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 25 °C
Versuchsvorschrift
(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 N2. 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 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.
Aufarbeitung
- temperatureto reflux for 3 h
- customthe solvent was removed
- additionmethanol was added
- stirringthe mixture was stirred
- filtrationfiltered
- concentrationthe filtrate was concentrated
- additionThe remaining oil was solidified by addition of hexane and ethanol
- stirringby stirring
- filtrationFinal filtration
- customdrying
- customresulted in pure 4-(2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-ylmethoxy)-butane-1-sulphonic acid sodium salt
Quellen und Nachweise
- ORD-Eintrag
- ord-8da8d49b223949588fe7763258526ffb
- Quelldatensatz
- uspto-grants-2006_12
- Patentnummer
- US07147936B2
Notizen zur Reaktion
Wird geladen…