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Benzene → HCID 13151225, Verbindung

HRID 905045
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 905045
S(Cl)(Cl)=O.[I:5][C:6]([I:12])=[C:7]([I:11])[C:8]([OH:10])=[O:9].N1C=CC=CC=1.[CH:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[I:11][C:7](=[C:6]([I:12])[I:5])[C:8]([O:10][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=[O:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 241Benzene2×HCID 1049PyridineHCID 24386Thionyl ChlorideHCID 53251402-Propenoic acid, 2,3,3-triiodo-

Produkt 1

HCID 13151225HCID 13151225, Verbindung

Versuchsvorschrift

A solution of 0.3 ml of thionyl chloride in 2 ml of benzene was added dropwise to a mixture of 0.3 g of triiodoacrylic acid, 0.3 ml of pyridine and 3 ml of benzene. The mixture was then stirred at room temperature for 45 minutes, after which the solvent was distilled off under reduced pressure. 5 ml of benzene and 0.3 ml of pyridine were added to the resulting residue, and then 0.3 g of phenol was added, with ice-cooling, after which the mixture was stirred at room temperature for 2 hours. At the end of this time, the reaction mixture was poured into an ice-cooled dilute solution of hydrochloric acid and then extracted with diethyl ether. The extract was washed, in turn, with a saturated aqueous solution of sodium bicarbonate, water and then a saturated aqueous solution of sodium chloride. The resulting solution was dried over anhydrous sodium sulphate and then the solvent was distilled off under reduced pressure. The resulting residue was purified by column chromatography through silica gel eluted with a 100:12 by volume mixture of hexane and ethyl acetate, to give 0.18 g of the title compound, melting at 83°-84.5° C.

Aufarbeitung

  1. distillationafter which the solvent was distilled off under reduced pressure
  2. addition5 ml of benzene and 0.3 ml of pyridine were added to the resulting residue
  3. addition0.3 g of phenol was added, with ice-
  4. temperaturecooling
  5. stirringafter which the mixture was stirred at room temperature for 2 hours
  6. additionAt the end of this time, the reaction mixture was poured into an ice-
  7. temperaturecooled dilute solution of hydrochloric acid
  8. extractionextracted with diethyl ether
  9. washThe extract was washed, in turn, with a saturated aqueous solution of sodium bicarbonate, water
  10. dry with materialThe resulting solution was dried over anhydrous sodium sulphate
  11. distillationthe solvent was distilled off under reduced pressure
  12. customThe resulting residue was purified by column chromatography through silica gel
  13. washeluted with a 100:12 by volume mixture of hexane and ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-7e05995589f9473ead3777f209c60b46
Quelldatensatz
uspto-grants-1983_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04421766

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