Reaktion #736888

ord-279744f9a4f14cb39654d967c3e65756

Reaktionsgleichung

O=[N+]([O-])c1ccccc1CO
2-nitrobenzyl alcohol
c1ccccc1
benzene
CCCCCCCCCCCCCCCCS(=O)(=O)Cl
hexadecanesulfonyl chloride
CCCCCCCCCCCCCCCCS(=O)(=O)OCc1ccccc1[N+](=O)[O-]
2-Nitrobenzyl hexadecanesulfonate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe mixture was evaporated to dryness in vacuo
  2. 2
    workup.ADDITIONthe solid taken up into a mixture of ether and water
  3. 3
    SonstigeThe ether layer was separated
  4. 4
    Trocknendried over MgSO4
  5. 5
    SonstigeEvaporation of the ether
  6. 6
    Sonstigegave a solid which
  7. 7
    Sonstigewas crystallized from absolute ethanol (yield 14.3 g, m.p. 63°-65° C.)

Vorschrift

To a stirred solution of 7.65 g (0.05 mol) of 2-nitrobenzyl alcohol in 75 ml of benzene containing 5.05 g (0.05 mol) of triethylamine was added 16.25 g (0.05 mol of hexadecanesulfonyl chloride. The mixture was stirred an additional four hours. The mixture was evaporated to dryness in vacuo and the solid taken up into a mixture of ether and water. The ether layer was separated and dried over MgSO4. Evaporation of the ether gave a solid which was crystallized from absolute ethanol (yield 14.3 g, m.p. 63°-65° C.).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04740600uspto-grants-1988_04