Reaktionsgleichung
[S:1]1[C:5]2[C:6]([C:10]([OH:12])=O)=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[N:2]1.CN(C)C=O.S(Cl)([Cl:20])=O>C1(C)C=CC=CC=1>[S:1]1[C:5]2[C:6]([C:10]([Cl:20])=[O:12])=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[N:2]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 85 °C
Versuchsvorschrift
290 g of benzo-1,2,3-thiadiazole-7-carboxylic acid are suspended in 1.6 l of toluene, 3.5 ml of dimethylformamide and 129 ml of thionyl chloride are added and the mixture is stirred at 80-90° C., the suspension turning into a solution as the release of gas progresses. When the reaction has ended, the solution is cooled and filtered over a little Hyflo, the residue is rinsed with toluene and the filtrate is evaporated. 297 g (93%) of crude acid chloride, which can be further reacted directly, result.
Aufarbeitung
- temperaturethe solution is cooled
- filtrationfiltered over a little Hyflo
- washthe residue is rinsed with toluene
- customthe filtrate is evaporated
- custom297 g (93%) of crude acid chloride, which can be further reacted directly
- customresult
Quellen und Nachweise
- ORD-Eintrag
- ord-5d5a961c60304c3ab9b10703a5dfae27
- Quelldatensatz
- uspto-grants-1999_12
- Patentnummer
- US06002013
Verknüpfte Notizen
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