Reaktion #367738

ord-0f970589eafc4013b0fddabf1e25ff9d

Reaktionsgleichung

COc1cc2c(cc1OC)S(=O)(=O)NC2=O
5,6-dimethoxysaccharin
CC[O+](CC)CC.F[B-](F)(F)F
triethyloxonium tetrafluoroborate
CCOC1=NS(=O)(=O)c2cc(OC)c(OC)cc21
title compound
CCOC1=NS(=O)(=O)c2cc(OC)c(OC)cc21
5,6-Dimethoxy-3-ethoxy-benzoisothiazole-1,1-dioxide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionAfter extraction with aqueous sodium bicarbonate
  2. 2
    Sonstigethe organic phase was dried
  3. 3
    Einengenconcentrated
  4. 4
    SonstigePurification by column chromatography (silica, chloroform)

Vorschrift

To a solution of 5,6-dimethoxysaccharin (0.8 g) in dichloromethane (100 ml) was added triethyloxonium tetrafluoroborate (3.5 ml, 1M soln in CH2Cl2) and the solution stirred at room temperature for 3 hrs. After extraction with aqueous sodium bicarbonate, the organic phase was dried and concentrated. Purification by column chromatography (silica, chloroform) gave the title compound (0.2 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04590192uspto-grants-1986_05