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4-Bromothiophenol → 1-Bromo-4-cyclopropylthiobenzene

HRID 549891
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 549891
[CH3:1][C:2]([CH3:5])([O-])C.[K+].[Br:7][C:8]1[CH:13]=[CH:12][C:11]([SH:14])=[CH:10][CH:9]=1.BrC1CC1>CS(C)=O.CCOCC>[Br:7][C:8]1[CH:13]=[CH:12][C:11]([S:14][CH:5]2[CH2:2][CH2:1]2)=[CH:10][CH:9]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 660494-BromothiophenolHCID 78037BromocyclopropaneHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 223501051-Bromo-4-cyclopropylthiobenzene

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 679Dimethyl SulfoxideLösungsmittelHCID 3283Diethyl Ether
Lösungsmittel

Versuchsvorschrift

To a degassed solution of potassium tert-butoxide (2.08 g, 18.51 mmol) in dry dimethylsulphoxide (6 mL), 4-bromo-benzenethiol (3.5 g, 18.5 mmol) was added and the mixture was stirred for 15 min at ambient temperature under nitrogen. Bromocyclopropane (4.4 mL, 55.5 mmol) was added afterwards and the reaction mixture was heated at 80° C. for 24 h in a sealed vessel. The mixture was cooled, diluted with ether (150 mL) and washed with water (100 mL). The aqueous layer was extracted with ether (3×50 mL). Combined organic extracts were finally dried with anhydrous magnesium sulfate. 1-Bromo-4-cyclopropylsulfanyl-benzene was obtained after evaporation of the solvent as yellow liquid.

Aufarbeitung

  1. temperaturethe reaction mixture was heated at 80° C. for 24 h in a sealed vessel
  2. temperatureThe mixture was cooled
  3. washwashed with water (100 mL)
  4. extractionThe aqueous layer was extracted with ether (3×50 mL)
  5. dry with materialCombined organic extracts were finally dried with anhydrous magnesium sulfate

Quellen und Nachweise

ORD-Eintrag
ord-4d49dc322caa43cab880af39e2ea9d06
Quelldatensatz
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07943613B2

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