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Ethanol → Ethyl 4-iodobenzoate

HRID 52439
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 52439
[I:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.S(Cl)(Cl)=O.[CH2:15](O)[CH3:16]>>[I:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH2:15][CH3:16])=[O:7])=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 702EthanolHCID 120854-Iodobenzoic acidHCID 24386Thionyl Chloride

Produkt 1

HCID 142891Ethyl 4-iodobenzoate

Versuchsvorschrift

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): 1.42 (3H, t, J~7 Hz), 4,4 (2H, q, J~7 Hz), 7.8 (4H).

Aufarbeitung

  1. temperaturethe mixture was then heated
Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion
  • temperatureat reflux for 3 hours
  • customSolvent was removed in vacuo
  • dissolutionthe residue was dissolved in 100 ml ether
  • washThe ether solution was washed with saturated NaHCO3 and saturated NaCl solutions
  • dry with materialdried (MgSO4)
  • customSolvent was then removed in vacuo
  • distillationthe residue kugelrohr distilled (100 degrees C; 0.55 mm)
  • Quellen und Nachweise

    ORD-Eintrag
    ord-1d78d00f34cd450f9f4a029dc2e84514
    Quelldatensatz
    uspto-grants-1997_04
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US05616712

    Notizen zur Reaktion

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