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Dichloromethane → 2,5-Dichloro-4-methylthiophene-3-sulfonyl chloride

HRID 8633
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 8633
[CH3:1][C:2]1[CH:6]=[CH:5][S:4]C=1.[S:7]([Cl:11])(Cl)(=[O:9])=[O:8].[Cl:12]S(O)(=O)=O.Cl[CH2:18][Cl:19]>>[Cl:12][C:5]1[S:4][C:18]([Cl:19])=[C:2]([CH3:1])[C:6]=1[S:7]([Cl:11])(=[O:9])=[O:8]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 6344Dichloromethane2×HCID 120243-MethylthiopheneHCID 24638Chlorosulfonic acidHCID 24648Sulfuryl chloride

Produkt 1

HCID 219837962,5-Dichloro-4-methylthiophene-3-sulfonyl chlorideAusbeute 25 %

Reaktionsbedingungen

Temperatur
10 °C

Versuchsvorschrift

To a cooled (10° C.) solution of 3-methylthiophene (5 g, 50 mmol) in dichloromethane (15 mL) was added a solution of sulfuryl chloride (8.6 mL) in dichloromethane (5 mL). The reaction mixture was maintained at 10° C. for 30 minutes, then at ambient temperature for 16 hours. The reaction was concentrated and redissolved in dichloromethane (30 mL) and cooled to −10° C. To the cooled solution was added chlorosulfonic acid (2 mL, 100 mmol). The reaction was maintained at −10° C. for 30 minutes, then at ambient temperature for 16 hours, at which time it was poured into ice water (50 mL) and extracted with dichloromethane (50 mL). The organic layer was dried (Mg2SO4) and concentrated to furnish a brown oil (3.3 g, 25%).

Aufarbeitung

  1. concentrationThe reaction was concentrated
  2. dissolutionredissolved in dichloromethane (30 mL)
  3. temperaturecooled to −10° C
  4. temperatureThe reaction was maintained at −10° C. for 30 minutes
  5. waitat ambient temperature for 16 hours
  6. extractionextracted with dichloromethane (50 mL)
  7. dry with materialThe organic layer was dried (Mg2SO4)
  8. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-d3a94c6cd2a949a99cb74eb9ff971a3b
Quelldatensatz
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07091204B2

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