Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[CH:16]=[CH:15][CH:14]=[CH:13][C:8]=2[C:9]([O:11]C)=[O:10])=[N:3][CH:2]=1.[ClH:17]>C(O)(=O)C>[ClH:17].[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[CH:16]=[CH:15][CH:14]=[CH:13][C:8]=2[C:9]([OH:11])=[O:10])=[N:3][CH:2]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of methyl 2-(pyrimidin-4-yl)benzoate (0.49 g), acetic acid (2.0 mL) and 6 N hydrochloric acid (10 mL) was heated under reflux for 5 hr. The solvent was evaporated under reduced pressure, and the obtained residue was washed with ethyl acetate to give the title compound (0.45 g).
Aufarbeitung
- temperaturewas heated
- temperatureunder reflux for 5 hr
- customThe solvent was evaporated under reduced pressure
- washthe obtained residue was washed with ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-93ddf8e9b2694f25803e12a7d3ebd9ae
- Quelldatensatz
- uspto-grants-2014_10
- Patentnummer
- US08865717B2
Verknüpfte Notizen
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