Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[OH:8].[Cl:9][CH2:10][C:11](Cl)=[O:12]>>[Cl:9][CH2:10][C:11]([NH:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[OH:8])=[O:12]Komponenten
3
Versuchsvorschrift
A solution of 4-amino-3-hydroxypyridine (7 g, 0.06 mol) and chloroacetyl chloride (50 ml) was refluxed for 2 hours, cooled and the excess solvent was removed by vacuum distillation. The crude material was dissolved in water, neutralized with Na2CO3 and the solid precipitated filtered and air dried to give the desired product, m.p. 155°-158° C. The structural assignment was supported by the proton NMR spectrum.
Aufarbeitung
- temperaturecooled
- customthe excess solvent was removed by vacuum distillation
- dissolutionThe crude material was dissolved in water
- customthe solid precipitated
- filtrationfiltered
- customair dried
Quellen und Nachweise
- ORD-Eintrag
- ord-0e717692545847bf99de662dd998060e
- Quelldatensatz
- uspto-grants-1997_07
- Patentnummer
- US05652363
Verknüpfte Notizen
Wird geladen…