Réaction #1318

ord-6724f220dc7c4e89ac64b79ac6a33d74

Équation de réaction

O=C(O)c1ccc(I)cc1
4-iodobenzoic acid
CCO
ethanol
O=S(Cl)Cl
thionyl chloride
CCOC(=O)c1ccc(I)cc1
title compound
CCOC(=O)c1ccc(I)cc1
Ethyl-4-iodobenzoate

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurethe mixture was then heated
  2. 2
    Températureat reflux for 3 hours
  3. 3
    AutreSolvent was removed in vacuo
  4. 4
    workup.DISSOLUTIONthe residue was dissolved in 100 ml ether
  5. 5
    LavageThe ether solution was washed with saturated NaHCO3 and saturated NaCl solutions
  6. 6
    Séchagedried (MgSO4)
  7. 7
    AutreSolvent was then removed in vacuo
  8. 8
    workup.DISTILLATIONthe residue kugelrohr distilled (100 degrees C.; 0.55 mm)

Mode opératoire

To a suspension of 10 g (40.32 mmol) of 4-iodobenzoic acid in 100 ml absolute ethanol was added 2 ml thionyl chloride and the mixture was then heated at reflux for 3 hours. Solvent was removed in vacuo and the residue was dissolved in 100 ml ether. The ether solution was washed with saturated NaHCO3 and saturated NaCl solutions and dried (MgSO4). Solvent was then removed in vacuo and the residue kugelrohr distilled (100 degrees C.; 0.55 mm) to give the title compound as a colorless oil, PMR (CDCl3): δ1.42 (3H, t, J~7 Hz), 4.4 (2H, q, J~7 Hz), 7.8 (4H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723620uspto-grants-1998_03