Hydrochloric Acid → Isopilocarpic Acid Sodium Salt
Reaktionsgleichung
[CH3:1][CH2:2][C@@H:3]1[C:7](=[O:8])[O:6][CH2:5][C@@H:4]1[CH2:9][C:10]1[N:14]([CH3:15])[CH:13]=[N:12][CH:11]=1.Cl.[OH-:17].[Na+:18].Cl>O>[CH3:1][CH2:2][C@@H:3]([C:7]([O-:6])=[O:8])[C@H:4]([CH2:5][OH:17])[CH2:9][C:10]1[N:14]([CH3:15])[CH:13]=[N:12][CH:11]=1.[Na+:18]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
Pilocarpine hydrochloride (3.92 g; 16.00 moles) was dissolved in distilled water (4 ml) and the solution was cooled to about 0° C. To the solution 18 ml of ice cold 2M NaOH were added in four portions. The solution was left standing at about 0° C. for one hour. After neutralizing excess NaOH with 5 ml of 1M HCl, the solution was evaporated under reduced pressure. The residue was dissolved in 60 ml of absolute ethanol and mixed for 10 minutes at 60° C. After cooling to 4° C. undissolved NaCl was removed by filtration. The filtrate was evaporated under reduced pressure, whereby 3.93 g of sodium pilocarpate were obtained as a white, extremely hygroscopic substance.
Aufarbeitung
- waitThe solution was left
- customthe solution was evaporated under reduced pressure
- dissolutionThe residue was dissolved in 60 ml of absolute ethanol
- additionmixed for 10 minutes at 60° C
- temperatureAfter cooling to 4° C. undissolved NaCl
- customwas removed by filtration
- customThe filtrate was evaporated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-d37ed0d5c9d84a7dab62e0522dee2f7f
- Quelldatensatz
- uspto-grants-1995_07
- Patentnummer
- US05436350
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