Dimethyl-3-nitrobiphenyl-4-malonate → 3-Nitro-biphenyl-4-acetic acid
Reaktionsgleichung
C[O:2][C:3](=[O:24])[CH:4]([C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:11][C:10]=1[N+:21]([O-:23])=[O:22])C(OC)=O>Cl>[N+:21]([C:10]1[CH:11]=[C:12]([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:13]=[CH:14][C:9]=1[CH2:4][C:3]([OH:24])=[O:2])([O-:23])=[O:22]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Crude dimethyl-3-nitrobiphenyl-4-malonate was refluxed in 30 mL of 6 N hydrochloric acid for 24 hours. The precipitate was collected by filtration, washed with water and dried to give 4.5 g of 3-nitrobiphenyl-4-acetic acid as a cream colored solid.
Aufarbeitung
- filtrationThe precipitate was collected by filtration
- washwashed with water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-716f03d1fcce4187968fed2164a70186
- Quelldatensatz
- uspto-grants-2001_11
- Patentnummer
- US06313158B1
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