Chlorosulfonic acid → 4-(2,2,2-Trifluoroacetamido)benzene-1-sulfonyl chloride
Reaktionsgleichung
[Cl:1][S:2]([OH:5])(=O)=[O:3].[F:6][C:7]([F:18])([F:17])[C:8]([NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:9]>>[F:6][C:7]([F:17])([F:18])[C:8]([NH:10][C:11]1[CH:16]=[CH:15][C:14]([S:2]([Cl:1])(=[O:5])=[O:3])=[CH:13][CH:12]=1)=[O:9]Komponenten
3
Versuchsvorschrift
Chlorosulfonic acid (100 g.) was cooled to 0° C. and trifluoroacetanilide (30 g.) was added portionwise with vigorous stirring keeping the temperature below +5° C. The reaction was stirred at room temperature overnight, and cautiously poured onto ice. The white solid produced was filtered, washed copiously with water, and dried to give 4-trifluoroacetamido benzenesulfonyl chloride (39.14 gl)(m.r. 143°-146° C.).
Aufarbeitung
- customthe temperature below +5° C
- stirringThe reaction was stirred at room temperature overnight
- additioncautiously poured onto ice
- customThe white solid produced
- filtrationwas filtered
- washwashed copiously with water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-ed5937b650f7415296cb11e2862453de
- Quelldatensatz
- uspto-grants-1988_12
- Patentnummer
- US04794196
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