Stannous Chloride → Ethyl 3-amino-5-bromobenzoate
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([CH:10]=[C:11]([N+:13]([O-])=O)[CH:12]=1)[C:5]([O:7][CH2:8][CH3:9])=[O:6].[Sn](Cl)Cl>C(O)C>[NH2:13][C:11]1[CH:10]=[C:4]([CH:3]=[C:2]([Br:1])[CH:12]=1)[C:5]([O:7][CH2:8][CH3:9])=[O:6]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of ethyl 3-bromo-5-nitrobenzoate (4.4 g, 16 mmol) and tin(II) chloride (40 g, 170 mmol) in ethanol (125 ml) was heated at 80° C. for 2 hours. The mixture was cooled to room temperature and the solvent evaporated. The residue was suspended in ethyl acetate (250 ml) and washed with 2M NaOH (2×250 ml). The organic phase was washed with water, dried and evaporated to give the title compound as a yellow solid (3.6 g, 92%)
Aufarbeitung
- customthe solvent evaporated
- washwashed with 2M NaOH (2×250 ml)
- washThe organic phase was washed with water
- customdried
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-330ae8d050ae46f99368cae8ef93dd31
- Quelldatensatz
- uspto-grants-2008_11
- Patentnummer
- US07446222B2
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