1,4-Butane sultone → Sodium 4-((2,3-dihydrothieno(3,4-b)(1,4)dioxin-2-yl)methoxy)butane-1-sulfonate

HRID 489589

Reaktionsgleichung

Reaktionsgleichung von HRID 489589
[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.[H-].[Na+:13].[CH2:14]1[S:19](=[O:21])(=[O:20])[O:18][CH2:17][CH2:16][CH2:15]1>O1CCCC1>[Na+:13].[O:1]1[CH:6]([CH2:7][O:8][CH2:17][CH2:16][CH2:15][CH2:14][S:19]([O-:21])(=[O:20])=[O:18])[CH2:5][O:4][C:3]2=[CH:9][S:10][CH:11]=[C:2]12

Komponenten

5

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 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 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

  1. temperatureto reflux for 3 h
  2. customthe solvent was removed
  3. additionmethanol was added
  4. stirringthe mixture was stirred
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated
  7. additionThe remaining oil was solidified by addition of hexane and ethanol
  8. stirringby stirring
  9. filtrationFinal filtration
  10. customdrying
  11. 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-690c6949eee1492aba64887b417a4129
Quelldatensatz
uspto-grants-2005_12
Patentnummer
US06977390B2

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