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4-Toluenesulfonyl chloride → 2-Tosylthiophene

HRID 507557
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 507557
[C:1]1([CH3:11])[CH:6]=[CH:5][C:4]([S:7](Cl)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[S:12]1[CH:16]=[CH:15][CH:14]=[CH:13]1>C(#N)C.[Cl-].[Zn+2].[Cl-]>[S:7]([C:13]1[S:12][CH:16]=[CH:15][CH:14]=1)([C:4]1[CH:5]=[CH:6][C:1]([CH3:11])=[CH:2][CH:3]=1)(=[O:9])=[O:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 73974-Toluenesulfonyl chlorideHCID 8030Thiophene

Produkt 1

HCID 2555212-TosylthiopheneAusbeute 95,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3007855ZincchlorideKatalysatorHCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

A mixture of p-toluenesulfonyl chloride (3 g, 15.7 mmol) and zinc chloride (3 g, 21.3 mmol) in acetonitrile (30 mL) was heated to reflux and thiophene (2.4 g, 28.5 mmol) was added dropwise. After refluxing for 4 h the mixture was cooled to rt and filtered through Celite. The filtrate was concentrated in vacuo and then 100 mL of sodium hydroxide (2 N) was added. The mixture was extracted with ethyl acetate (3×60 mL) and the combined organic layers were washed with hydrochloric acid (10%, 50 mL) and brine (100 mL), dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated in vacuo and the product was purified by flash chromatography eluting with dichloromethane/hexane (2:3) to give the title compound (0.54 g, 15 mmol).

Aufarbeitung

  1. temperaturewas heated
  2. temperatureto reflux
  3. temperatureAfter refluxing for 4 h the mixture
  4. filtrationfiltered through Celite
  5. concentrationThe filtrate was concentrated in vacuo
  6. addition100 mL of sodium hydroxide (2 N) was added
  7. extractionThe mixture was extracted with ethyl acetate (3×60 mL)
  8. washthe combined organic layers were washed with hydrochloric acid (10%, 50 mL) and brine (100 mL)
  9. dry with materialdried over anhydrous magnesium sulfate
  10. filtrationfiltered
  11. customThe solvent was evaporated in vacuo
  12. customthe product was purified by flash chromatography
  13. washeluting with dichloromethane/hexane (2:3)

Quellen und Nachweise

ORD-Eintrag
ord-4e7e103c822847318f71eb53a058a850
Quelldatensatz
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07786132B2

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