Hydrochloric Acid → 1,8-Diazabicyclo[5.4.0]undec-7-ene hydrochloride
Reaktionsgleichung
[CH2:1]1[CH2:11][CH2:10][N:9]2[C:4](=[N:5][CH2:6][CH2:7][CH2:8]2)[CH2:3][CH2:2]1.[ClH:12]>CCOCC>[ClH:12].[CH2:1]1[CH2:11][CH2:10][N:9]2[C:4](=[N:5][CH2:6][CH2:7][CH2:8]2)[CH2:3][CH2:2]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A flame dried flask was charged with DBU (1.0 g, 6.56 mmol), ether (20 mL) and a stirbar under dry nitrogen atmosphere. With vigorous stirring, a 1M ethereal HCl solution (6.6 mL, 6.6 mmol) was added to form a white precipitate. Stirring was continued for 1 hour then excess solvent was decanted to yield 1.1 g (90%). The salt was then dried under high vacuum.
Aufarbeitung
- customA flame dried flask
- customto form a white precipitate
- customexcess solvent was decanted
- customto yield 1.1 g (90%)
- customThe salt was then dried under high vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-9b0482f393374961a752c91ce87c0658
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08846851B2
Notizen zur Reaktion
Wird geladen…