Réaction #66017

ord-54b763fa48f0470b873aab1b94d435ed

Équation de réaction

O=S(=O)(O)c1ccc(Oc2ccccc2)cc1
sulphonic acid
O=S(=O)(O)c1ccc(Oc2ccccc2)cc1
4-phenoxybenzenesulphonic acid
O=S(Cl)Cl
thionyl chloride
O=S(=O)(Cl)c1ccc(Oc2ccccc2)cc1
4-Phenoxy-benzenesulphonyl chloride

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureat reflux
  2. 2
    AutreThe solvent was evaporated
  3. 3
    workup.DISSOLUTIONthe residue dissolved in Et20 (40 mL)
  4. 4
    LavageThe ether solution was washed with 5% aqueous NaOH (3×40 mL) and water (6×40 mL)
  5. 5
    Séchagedried over anhydrous MgSO4
  6. 6
    Filtrationfiltered
  7. 7
    Concentrationconcentrated in vacuo
  8. 8
    AutreAfter drying in high vacuum overnight
  9. 9
    Autrethe pure product was obtained as a white solid

Mode opératoire

The sulphonic acid (2a) was dissolved in an excess of thionyl chloride (30 mL), a catalytic amount of DMF (cat) was added, and the resulting mixture was stirred for 6 h at reflux. The solvent was evaporated and the residue dissolved in Et20 (40 mL). The ether solution was washed with 5% aqueous NaOH (3×40 mL) and water (6×40 mL), dried over anhydrous MgSO4, filtered, and concentrated in vacuo. After drying in high vacuum overnight, the pure product was obtained as a white solid. Yield 63%: 2.09 g, 7.44 mmol, (light yellow syrup). 1H-NMR (CDCl3): δ 7.44 (d, 3J=9.1 Hz, 2H, ArH), 7.38 (d, 3J=9.1 Hz, 2H, ArH), 7.19 (t, 1H, ArH), 7.12 (d, 3J=9.1 Hz, 2H, ArH), 6.98 (d, 3J=9.1 Hz, 2H, ArH)

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08524194B2uspto-grants-2013_09