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p-Toluenesulfonic acid → HCID 23291432, Verbindung

HRID 365394
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 365394
[S:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[C:11]([O:13][CH3:14])=[O:12])[CH:4](O)[CH2:3][CH2:2]1.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[CH3:14][O:13][C:11]([C:9]1[CH:8]=[CH:7][CH:6]=[C:5]2[C:10]=1[S:1][CH2:2][CH:3]=[CH:4]2)=[O:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 6101p-Toluenesulfonic acidHCID 53944516HCID 53944516, Verbindung

Produkt 1

HCID 23291432HCID 23291432, VerbindungAusbeute 87,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

Methyl thiochroman-4-ol-8-carboxylate (0.337 g, 1.50 mmol) was dissolved in toluene (25 ml) and was treated with p-toluenesulphonic acid (0.028 g, 0.15 mmol). The mixture was then heated to reflux with stirring. After 2 h, the reaction mixture was allowed to cool and was washed with sodium hydrogen carbonate solution. The aqueous layer was then extracted with EtOAc (1×), and the combined organic layers were dried (Na2SO4) and evaporated under reduced pressure to give a pale yellow oil which was purified by silica-gel chromatography (pentane: Et2O 2:1 as eluant) to give the title compound (D2b) as a pale yellow oil (0.270 g, 87%)

Aufarbeitung

  1. temperatureThe mixture was then heated
  2. temperatureto reflux
  3. temperatureto cool
  4. washwas washed with sodium hydrogen carbonate solution
  5. extractionThe aqueous layer was then extracted with EtOAc (1×)
  6. dry with materialthe combined organic layers were dried (Na2SO4)
  7. customevaporated under reduced pressure
  8. customto give a pale yellow oil which
  9. customwas purified by silica-gel chromatography (pentane: Et2O 2:1 as eluant)

Quellen und Nachweise

ORD-Eintrag
ord-94768fded6524726a191294fe9c28b96
Quelldatensatz
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06127379

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