Chlorosulfonic acid → 4-(2-Sulfamoylethyl)benzenesulfonyl chloride

HRID 1173100Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1173100
[C:1]1([CH2:7][CH2:8][S:9]([NH2:12])(=[O:11])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:13][S:14](O)(=[O:16])=[O:15]>>[S:9]([CH2:8][CH2:7][C:1]1[CH:2]=[CH:3][C:4]([S:14]([Cl:13])(=[O:16])=[O:15])=[CH:5][CH:6]=1)(=[O:10])(=[O:11])[NH2:12]

Komponenten

3

Versuchsvorschrift

1.3 g (7.3 mmol) of 2-phenylethanesulfonamide was added to 2.4 g (36.5 mmol) of chlorosulfonic acid under ice-cooling over 20 minutes, followed by stirring at room temperature for further 90 minutes. The reaction mixture solution was poured into ice-water, and then extracted with ethyl acetate. The extract was successively washed with an aqueous saturated sodium bicarbonate and brine, and dried over magnesium sulfate. The solvent was evaporated, to give 1.6 g of the title compound.

Aufarbeitung

  1. temperaturecooling over 20 minutes
  2. extractionextracted with ethyl acetate
  3. washThe extract was successively washed with an aqueous saturated sodium bicarbonate and brine
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-9ec12645fce04357a1abc45e77bdeb35
Quelldatensatz
uspto-grants-2010_11
Patentnummer
US07834049B2

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