Benzonitrile, 4-bromo- → 4-Bromo-N-hydroxybenzimidamide
Reaktionsgleichung
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1.Cl.[NH2:11][OH:12].CCN(C(C)C)C(C)C>C(O)C>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([C:6](=[N:11][OH:12])[NH2:7])=[CH:4][CH:3]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 90 °C
Versuchsvorschrift
To a solution of 4-bromobenzonitrile (5.0 g, 27.5 mmol) in ethanol (42 ml) at room temperature, hydroxylamine hydrochloride (1.91 g, 27.5 mmol) and DIPEA (4.8 ml, 27.5 mmol) were added. The reaction mixture was stirred at 90° C. for 5 hours. After cooled to room temperature, the resulting mixture was concentrated to yield a colorless viscous liquid. The liquid was extracted with ethyl acetate and the organic layer was dried over magnesium sulfate, filtered and then concentrated to give a crude compound, which was washed with n-hexane to yield product 15 as a white solid (5.0 g).
Aufarbeitung
- temperatureAfter cooled to room temperature
- concentrationthe resulting mixture was concentrated
- customto yield a colorless viscous liquid
- extractionThe liquid was extracted with ethyl acetate
- dry with materialthe organic layer was dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto give a crude compound, which
- washwas washed with n-hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-3a6f27639a944d6f898938c65c4a7fb1
- Quelldatensatz
- uspto-grants-2013_04
- Patentnummer
- US08415482B2
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