Reaktionsgleichung
Cl.[CH3:2][C:3]1[C:8]2[C:9](=[O:14])[NH:10][S:11](=[O:13])(=[O:12])[C:7]=2[CH:6]=[CH:5][C:4]=1N.N([O-])=O.[Na+].[I-:20].[K+]>O.C(O)(=O)C>[CH3:2][C:3]1[C:8]2[C:9](=[O:14])[NH:10][S:11](=[O:13])(=[O:12])[C:7]=2[CH:6]=[CH:5][C:4]=1[I:20]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 50 °C
Versuchsvorschrift
A mixture of 205 ml of glacial acetic acid, 160 ml of water and 40 ml of conc. HCl is initially taken and 23.4 g (0.11 mol) of 4-methyl-5-amino-1,1,3-trioxo-2,3-dihydro-1λ6 benz[d]isothiazole are introduced with stirring at 15°-20° C. 7.9 g (0.115 mol) of sodium nitrite are added dropwise to the resulting suspension at 5°-10° C. and it is stirred at 5° C. for 30 min. The diazonium salt, which is present as a suspension, is then added dropwise in portions to a solution of 19.1 g (0.115 mol) of potassium iodide in 170 ml of water which is warmed to 50° C., nitrogen being formed. After cooling to room temperature, the deposited product is isolated by filtering off with suction, washed with water and dried under reduced pressure at 50° C. 32.5 g (0.1 mol=91% of theory) of a solid of m.p.: 257°-258° C. are obtained. A combustion analysis gave an iodine content of 38.5% (theory 39.3%).
Aufarbeitung
- stirringit is stirred at 5° C. for 30 min
- customnitrogen being formed
- temperatureAfter cooling to room temperature
- customthe deposited product is isolated
- filtrationby filtering off with suction
- washwashed with water
- customdried under reduced pressure at 50° C
- custom32.5 g (0.1 mol=91% of theory) of a solid of m.p.: 257°-258° C. are obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-7fc91a129aeb4cb09cfa6ba7c7b4f71f
- Quelldatensatz
- uspto-grants-1999_01
- Patentnummer
- US05863864
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