Reaktion #43888

ord-ba1f189d3ecd43818b020a5a70fbedfa

Reaktionsgleichung

CCOC(=O)c1ccc(S(=O)(=O)[O-])cc1.[K+]
potassium 4-ethoxycarbonylbenzenesulfonate
O=P(Cl)(Cl)Cl
POCl3
CCOC(=O)c1ccc(S(=O)(=O)Cl)cc1
white solid
CCOC(=O)c1ccc(S(=O)(=O)Cl)cc1
4-Ethoxycarbonylbenzenesulfonyl Chloride

Lösungsmittel

Reaktionsbedingungen

Temperatur
75°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA round bottom flask, fitted with a magnetic stir bar and a hose adapter
  2. 2
    Temperaturto cool to room temperature
  3. 3
    Einengenwas then concentrated
  4. 4
    Sonstigea rotary evaporator
  5. 5
    TemperaturThe flask was then cooled in an ice bath
  6. 6
    workup.ADDITIONice was added to the mixture in the flask
  7. 7
    SonstigeThe product crystallized as a white solid
  8. 8
    Filtrationwas filtered
  9. 9
    Waschenwashed
  10. 10
    SonstigeThe product was dried under vacuum at room temperature

Vorschrift

A round bottom flask, fitted with a magnetic stir bar and a hose adapter connected to a source of nitrogen gas, was charged with a solution of potassium 4-ethoxycarbonylbenzenesulfonate (75.1 g) dissolved in a 3:1 (v/v) mixture of acetonitrile (300 mL) and sulfolane (100 mL). As the solution was stirred, POCl3 (55 mL) was added slowly and the stirring mixture was heated at 75° C. under a nitrogen atmosphere for 3 hours. The heterogeneous reaction mixture was allowed to cool to room temperature and was then concentrated using a rotary evaporator. The flask was then cooled in an ice bath and ice was added to the mixture in the flask. The product crystallized as a white solid and was filtered and washed with cold deionized water. The product was dried under vacuum at room temperature and 3 mmHg for 2 hours to afford 76 g of white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732633B2uspto-grants-2010_06