(1,1'-Biphenyl)-3-ol, 4-nitro- → 2-Amino-5-phenylphenol
Reaktionsgleichung
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][C:5]=1[OH:16])([O-])=O>C(O)C.[Pd]>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][C:5]=1[OH:16]Komponenten
4
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
8.8 g (40 mmol) of 4-nitro-1,1′-biphenyl-3-ol from step B was dissolved in 120 mL of ethanol and hydrogenated in the presence of 0.8 g of a palladium-activated carbon catalyst (10%) at 25° C. After the required quantity of hydrogen had been absorbed, the catalyst was filtered off, and the solvent was distilled off in a rotary evaporator. This gave 7.3 g of 4° amino-1,1′-biphenyl-3-ol.
Aufarbeitung
- customAfter the required quantity of hydrogen had been absorbed
- filtrationthe catalyst was filtered off
- distillationthe solvent was distilled off in a rotary evaporator
- customThis gave 7.3 g of 4° amino-1,1′-biphenyl-3-ol
Quellen und Nachweise
- ORD-Eintrag
- ord-6df45d51665c49f09d124502c444021a
- Quelldatensatz
- uspto-grants-2006_10
- Patentnummer
- US07122061B2
Notizen zur Reaktion
Wird geladen…