Reaktion #1914819

ord-cd186954ca404a55bd09c2108542bbe0

Reaktionsgleichung

OCC1COc2cscc2O1
(2,3-Dihydro-thieno[3,4-b][1,4]dioxin-2-yl)-methanol
[H-].[Na+]
NaH
O=S1(=O)CCCCO1
butanesultone
O=S(=O)([O-])CCCCOCC1COc2cscc2O1.[Na+]
4-(2,3-dihydro-thieno[3,4-b][1,4]dioxin-2-yl-methoxy)-butane-1-sulphonic acid sodium salt

Lösungsmittel

Reaktionsbedingungen

Temperatur
25°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto reflux for 3 h
  2. 2
    Sonstigethe solvent was removed
  3. 3
    workup.ADDITIONmethanol 5 was added
  4. 4
    workup.STIRRINGthe mixture was stirred
  5. 5
    Filtrationfiltered
  6. 6
    Einengenthe filtrate was concentrated
  7. 7
    workup.ADDITIONThe remaining oil was solidified by addition of hexane and ethanol
  8. 8
    workup.STIRRINGby stirring
  9. 9
    FiltrationFinal filtration
  10. 10
    Sonstigedrying
  11. 11
    Sonstigeresulted 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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07056600B2uspto-grants-2006_06