Hydrochloric Acid → HCID 20316840, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[CH:10]=[C:9]([C:11]([OH:13])=[O:12])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.Cl[C:15]1[CH:23]=[CH:22][C:18]([C:19]([OH:21])=[O:20])=[CH:17][N:16]=1.Cl.[CH2:25](O)[CH3:26]>>[C:11]([C:9]1[CH:10]=[C:2]2[C:3]([C:4](=[O:6])[N:16]3[CH:17]=[C:18]([C:19]([OH:21])=[O:20])[CH:22]=[CH:23][C:15]3=[N:1]2)=[CH:7][CH:8]=1)([O:13][CH2:25][CH3:26])=[O:12]Komponenten
5
Versuchsvorschrift
A mixture of 2.00g (11.1 mmol) of 2-aminoterephthalic acid, 1.73g (11.1 mmol) of 6-chloronicotinic acid, 2.5ml of conc. HCl and 25ml of ethanol was heated at reflux for 67 hours. The mixture was cooled and filtered to give 0.90g of solid, mp. 275° -324° . The crude material was recrystallized from 1-propanol and gave 0.40g of the mono-esterified product, mp. 283° -293° dec.
Aufarbeitung
- temperaturewas heated
- temperatureat reflux for 67 hours
- temperatureThe mixture was cooled
- filtrationfiltered
Quellen und Nachweise
- ORD-Eintrag
- ord-786c7e3119be47bea74c438f57a1faf2
- Quelldatensatz
- uspto-grants-1977_07
- Patentnummer
- US04033961
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