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Hydrofluoric Acid → 2-Phenyl-10-anthrone

HRID 68513
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 68513
C1C2C(=CC=CC=2)C=CC=1[C:11]1[CH:12]=[C:13]([CH:24]=[CH:25][CH:26]=1)[CH2:14][C:15]1[CH:23]=[CH:22][CH:21]=[CH:20][C:16]=1[C:17]([OH:19])=O.F>>[C:11]1([C:11]2[CH:26]=[CH:25][C:24]3[C:17](=[O:19])[C:16]4[C:15](=[CH:23][CH:22]=[CH:21][CH:20]=4)[CH2:14][C:13]=3[CH:12]=2)[CH:12]=[CH:13][CH:24]=[CH:25][CH:26]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 14917Hydrofluoric Acid2×HCID 58194347HCID 58194347, Verbindung

Produkt 1

HCID 670655092-Phenyl-10-anthroneAusbeute 144,7 %

Versuchsvorschrift

First, 11.7 g of 2-[3-(2-naphthyl)benzyl]benzoic acid were added to 250 mL of liquid hydrogen fluoride, and then the mixture was stirred until hydrogen fluoride evaporated. The residue was dissolved in chloroform, and then the solution was sequentially washed with water, an aqueous solution of ammonium hydroxide, and water. After the chloroform solution had been dried with magnesium sulfate, the solvent was removed by distillation under reduced pressure. The residue was crystallized with methanol, and was then recrystallized with cyclohexane and acetone. Thus, 6.76 g of 2-phenyl-10-anthrone were obtained (in 61% yield).

Aufarbeitung

  1. customevaporated
dissolution
The residue was dissolved in chloroform
  • washthe solution was sequentially washed with water
  • dry with materialAfter the chloroform solution had been dried with magnesium sulfate
  • customthe solvent was removed by distillation under reduced pressure
  • customThe residue was crystallized with methanol
  • customwas then recrystallized with cyclohexane and acetone
  • Quellen und Nachweise

    ORD-Eintrag
    ord-24756ba125c844d58954503471391797
    Quelldatensatz
    uspto-grants-2014_09
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US08822041B2

    Notizen zur Reaktion

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