Nitric Acid → 2-Bromo-5-nitrobenzaldehyde
Reaktionsgleichung
[N+:1]([O-:4])(O)=[O:2].[Br:5][C:6]1[CH:13]=[CH:12][CH:11]=[CH:10][C:7]=1[CH:8]=[O:9]>OS(O)(=O)=O>[Br:5][C:6]1[CH:13]=[CH:12][C:11]([N+:1]([O-:4])=[O:2])=[CH:10][C:7]=1[CH:8]=[O:9]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A nitrating acid prepared at -10° C. by adding 55 ml of concentrated H2SO4 to 20 ml of 98 percent HNO3 was added dropwise, in the course of 60 minutes, to a solution of 63.4 g (0.34 mole) of 2-bromobenzaldehyde in 110 ml of concentrated H2SO4 at -5° C. Stirring was continued for a further 45 minutes, after which the reaction mixture was poured onto 550 g of ice, and the precipitated solid was filtered off under suction, washed with water, then with 10 percent strength Na2CO3 solution and again with water. Drying under reduced pressure at 50° C. gave 72 g (92% of theory) of product as a yellow solid of melting point 86°-88° C.
Aufarbeitung
- customA nitrating acid prepared at -10° C.
- filtrationthe precipitated solid was filtered off under suction
- washwashed with water
- customDrying under reduced pressure at 50° C.
- customgave 72 g (92% of theory) of product as a yellow solid of melting point 86°-88° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-1dba62bde5014a4db694683de5dcac08
- Quelldatensatz
- uspto-grants-1993_08
- Patentnummer
- US05237089
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