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Thionyl Chloride → 2-Cyclopentylethane-1-sulfonyl chloride

HRID 433892
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 433892
[Na+].[CH:2]1([CH2:7][CH2:8][S:9]([O-:12])(=O)=[O:10])[CH2:6][CH2:5][CH2:4][CH2:3]1.S(Cl)([Cl:15])=O>CN(C)C=O>[CH:2]1([CH2:7][CH2:8][S:9]([Cl:15])(=[O:12])=[O:10])[CH2:6][CH2:5][CH2:4][CH2:3]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 24386Thionyl ChlorideHCID 880142572-(Cyclopentyl)ethylsulfonic acid sodium salt

Produkt 1

HCID 187560792-Cyclopentylethane-1-sulfonyl chloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideKatalysator

Versuchsvorschrift

Dimethylformamide (5 drops) was added over 1 minute to a stirred solution of 2-(cyclopentyl)ethylsulfonic acid sodium salt (1 5.5 g, 87.5 mmol) in thionyl chloride (60 ml) under a nitrogen atmosphere. The reaction mixture was stirred under reflux for 5 hours and was then cooled to room temperature and concentrated under vacuum. The residue was suspended in toluene (100 ml) and then concentrated under vacuum. The residue was dissolved in a mixture of ethyl acetate (150 ml) and water (150 ml) and the organic phase was separated. The aqueous phase was extracted with ethyl acetate (100 ml) and the combined organic extracts were washed with brine (3×100 ml), dried (magnesium sulfate) and evaporated to give the title compound as a brown oil (14.1 g), Rf 0.5 (pentane/ethyl acetate 95:5).

Aufarbeitung

  1. temperatureunder reflux for 5 hours
  2. concentrationconcentrated under vacuum
  3. concentrationconcentrated under vacuum
  4. dissolutionThe residue was dissolved in a mixture of ethyl acetate (150 ml) and water (150 ml)
  5. customthe organic phase was separated
  6. extractionThe aqueous phase was extracted with ethyl acetate (100 ml)
  7. washthe combined organic extracts were washed with brine (3×100 ml)
  8. dry with materialdried (magnesium sulfate)
  9. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-dc6ab3b7ef9c4b9d9c760a52f8914e1f
Quelldatensatz
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06670362B2

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