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Potassium Carbonate → 2-Methyl-4-(2,5-dimethylphenyl)thio-2-butene

HRID 974827
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 974827
Br[CH2:2][CH:3]=[C:4]([CH3:6])[CH3:5].C(=O)([O-])[O-].[K+].[K+].[CH3:13][C:14]1[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][C:15]=1[SH:21]>CC(C)=O>[CH3:5][C:4](=[CH:3][CH2:2][S:21][C:15]1[CH:16]=[C:17]([CH3:20])[CH:18]=[CH:19][C:14]=1[CH3:13])[CH3:6]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 700922-Butene, 1-bromo-3-methyl-HCID 776152,5-Xylenethiol

Produkt 1

HCID 129936832-Methyl-4-(2,5-dimethylphenyl)thio-2-buteneAusbeute 100,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Versuchsvorschrift

80 ml of acetone, 9.1 g (0.06 mol) of 1-bromo-3-methyl-2-butene and 8.0 g (0.058 mol) of anhydrous potassium carbonate were added to 8.0 g (0.058 mol) of 2,5-dimethylthiophenol, and the mixture was refluxed under heat for 1 hour. After the completion of the reaction, a formed salt was removed by filtration, and the acetone was distilled off under reduced pressure. Then, ethyl acetate was added to the residue, and the mixture was washed with a saturated sodium chloride aqueous solution. The mixture was dried over anhydrous sodium sulfate, and then the ethylacetate was distilled off to give 12 g (yield 100%) of 2-methyl-4-(2,5-dimethylphenyl)thio-2-butene.

Aufarbeitung

  1. temperaturethe mixture was refluxed
  2. temperatureunder heat for 1 hour
  3. customAfter the completion of the reaction
  4. customa formed salt was removed by filtration
  5. distillationthe acetone was distilled off under reduced pressure
  6. additionThen, ethyl acetate was added to the residue
  7. washthe mixture was washed with a saturated sodium chloride aqueous solution
  8. dry with materialThe mixture was dried over anhydrous sodium sulfate
  9. distillationthe ethylacetate was distilled off

Quellen und Nachweise

ORD-Eintrag
ord-1b929ff26abe44fb8a7cb974cf95e3fe
Quelldatensatz
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05607898

Notizen zur Reaktion

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