Reaktion #11345

ord-7c7f331849e741a384a746489950e6cd

Reaktionsgleichung

c1ccc2c(c1)OCO2
1,3-benzodioxole
O=S(=O)(Cl)Cl
sulfuryl chloride
O=S(=O)(Cl)c1ccc2c(c1)OCO2
(1,3-benzodioxol-5-yl)sulfonyl chloride
Ausbeute 16.3%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewhereupon a solid formed
  2. 2
    TemperaturThe reaction was cooled
  3. 3
    Extraktionextracted with methylene chloride
  4. 4
    Trocknendried over magnesium sulfate
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated
  7. 7
    Sonstigeto give 7.32 g of crude material as a black oil
  8. 8
    SonstigeThis was chromatographed on silica gel using 20% methylene chloride/hexane

Vorschrift

To a solution of 4.25 g of anhydrous N,N-dimethylformamide at 0° C. under nitrogen was added 7.84 g of sulfuryl chloride, whereupon a solid formed. After stirring for 15 minutes, 6.45 g of 1,3-benzodioxole was added, and the mixture heated at 100° C. for 2 hours. The reaction was cooled, poured into ice water, extracted with methylene chloride, dried over magnesium sulfate, filtered and concentrated to give 7.32 g of crude material as a black oil. This was chromatographed on silica gel using 20% methylene chloride/hexane to afford 1.9 g of (1,3-benzodioxol-5-yl)sulfonyl chloride.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07098202B2uspto-grants-2006_08