Reaktion #4584

ord-983466e81fae4be2b37209716d2579ca

Reaktionsgleichung

CC(=O)COc1ccccc1S(N)(=O)=O
2-(2-propanon-1-yloxy)phenylsulfonamide
OCCO
ethylene glycol
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
Cc1ccccc1
toluene
CC1(COc2ccccc2S(N)(=O)=O)OCCO1
2-(2-methyl-1,3-dioxolan-2-yl-methoxy)phenylsulfonamide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturis heated for 7 hours
  2. 2
    Temperaturto reflux
  3. 3
    Sonstigewhile simultaneously separating
  4. 4
    Sonstigethe water of reaction
  5. 5
    Waschenthe organic phase is washed with saturated sodium bicarbonate solution and water
  6. 6
    Sonstigedried
  7. 7
    Einengenconcentrated

Vorschrift

A mixture of 4.58 g of 2-(2-propanon-1-yloxy)phenylsulfonamide, 2 ml of ethylene glycol, 0.02 g of p-toluenesulfonic acid and 30 ml of toluene is heated for 7 hours to reflux while simultaneously separating the water of reaction. The cooled solution is taken up in 80 ml of ethyl acetate and the organic phase is washed with saturated sodium bicarbonate solution and water, dried and concentrated, affording 5 g of 2-(2-methyl-1,3-dioxolan-2-yl-methoxy)phenylsulfonamide in the form of a yellow viscous oil which can be further used without purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04726836uspto-grants-1988_02