Reaktionsgleichung
[CH3:1][O:2][CH2:3][C:4]1[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=1[NH2:6].[N:11]([O-])=O.[Na+].[OH-].[Na+]>Cl.O>[CH3:1][O:2][CH2:3][C:4]1[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=1[NH:6][NH2:11]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- -10 °C
Versuchsvorschrift
6.86 g (50 m moles) of 2-methoxymethylaniline was dissolved in 50 ml of concentrated hydrochloric acid. The solution was cooled to −10° C. Thereto was dropwise added a solution of sodium nitrite (4.14 g, 60 m moles) dissolved in water (50 ml) while a temperature of −10° C. to 0° C. was being kept. Then, a solution of 44.6 g (235 m moles) of stannous chloride dissolved in concentrated hydrochloric acid (50 ml) was dropwise added at the above temperature in 1 hour. After the completion of the dropwise addition, stirring was conducted with a gradual temperature increase to about 20° C. Then, a 10% aqueous sodium hydroxide solution was dropped to obtain a pH of 14, after which extraction with toluene was conducted. The toluene layer was washed with water and concentrated under reduced pressure using a rotary evaporator to obtain 5.40 g (35.5 m moles) of liquid 2-methoxymethylphenylhydrazine. Yield: 71%.
Aufarbeitung
- additionwas dropwise added at the above temperature in 1 hour
- additionAfter the completion of the dropwise addition
- temperatureincrease to about 20° C
- customto obtain a pH of 14
- extractionafter which extraction with toluene
- washThe toluene layer was washed with water
- concentrationconcentrated under reduced pressure
- customa rotary evaporator
Quellen und Nachweise
- ORD-Eintrag
- ord-bff5a41a01c241e79c1ed5d9deae2027
- Quelldatensatz
- uspto-grants-2007_09
- Patentnummer
- US07271263B2
Verknüpfte Notizen
Wird geladen…