Hydrochloric Acid → 4-Chloro-3-(chlorosulphonyl)benzoic acid
Reaktionsgleichung
[Cl:1][S:2]([OH:5])(=O)=[O:3].[Cl:6][C:7]1[CH:15]=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[CH:9][CH:8]=1.Cl>O>[Cl:6][C:7]1[CH:15]=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[CH:9][C:8]=1[S:2]([Cl:1])(=[O:5])=[O:3]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
28.05 kg (16 l) of chlorosulfonic acid are initially introduced and 4.4 kg of 4-chlorobenzoic acid were added in the course of 10 minutes with stirring (no heat effect). In the course of 90 minutes, the mixture was heated to 130-135° C., during which evolution of HCl was to be observed. The mixture was subsequently stirred for 3 hours at the stated temperature, and allowed to cool and to stand overnight. The reaction mixture was then allowed to run with stirring onto a mixture of 70 kg of ice and 30 kg of water, during which the temperature must not climb above 10° C. The product was filtered off with suction, washed with 40 kg of water and dried in vacuo at 40° C.
Aufarbeitung
- stirringThe mixture was subsequently stirred for 3 hours at the stated temperature
- temperatureto cool
- customclimb above 10° C
- filtrationThe product was filtered off with suction
- washwashed with 40 kg of water
- customdried in vacuo at 40° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-cf9417b569df4750a0f842de6adaa6f3
- Quelldatensatz
- uspto-grants-2000_02
- Patentnummer
- US06022899
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