Potassium Hydroxide → 5-Bromosalicylhydroxamic acid
Reaktionsgleichung
[OH-:1].[K+].[Br:3][C:4]1[CH:18]=[C:8]([C:9](OC2C=CC=CC=2)=[O:10])[C:7]([OH:19])=[CH:6][CH:5]=1.Cl.[NH2:21]O>CO>[Br:3][C:4]1[CH:18]=[C:8]([C:9]([NH:21][OH:1])=[O:10])[C:7]([OH:19])=[CH:6][CH:5]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A methanol solution of 127 g of KOH was gradually added to a methanol solution of 210 g of phenyl 5-bromosalicylate prepared as in (2-1) above and 105 g of hydroxylamine hydrochloride. After stirring for 4 hours, the precipitate formed was collected by filtration. The precipitation was then suspended in water, and 60 ml of conc. hydrochloric acid (35%) was added thereto, followed by stirring for two hours to collect the precipitate by filtration followed by drying. Yield: 136 g.
Aufarbeitung
- customthe precipitate formed
- filtrationwas collected by filtration
- customThe precipitation
- addition60 ml of conc. hydrochloric acid (35%) was added
- stirringby stirring for two hours
- customto collect the precipitate
- filtrationby filtration
- customby drying
Quellen und Nachweise
- ORD-Eintrag
- ord-b221f47e46fb4456a9cee6c90c3f2d22
- Quelldatensatz
- uspto-grants-1987_01
- Patentnummer
- US04637902
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