Hydrochloric Acid → 4-(3-Methylphenyl)-4-hydroxypiperidine hydrochloride
Reaktionsgleichung
C(OC([N:8]1[CH2:13][CH2:12][C:11]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([CH3:21])[CH:16]=2)([OH:14])[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:22]>CCOC(C)=O>[ClH:22].[CH3:21][C:17]1[CH:16]=[C:15]([C:11]2([OH:14])[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]2)[CH:20]=[CH:19][CH:18]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of N-t-butoxycarbonyl-4-(3-methylphenyl)-4-hydroxy piperidine (0.546 mg, 1.87 mmol) in EtOAc (30 ml) at 0° C. was bubbled gasseous HCl until saturated. After 10 min the solvent was evaporated in vacuo to afford the title compound of sufficient purity to be used in the next step.
Aufarbeitung
- customAfter 10 min the solvent was evaporated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-8446683b209e4700a6482f9df30aa441
- Quelldatensatz
- uspto-grants-1999_04
- Patentnummer
- US05891889
Notizen zur Reaktion
Wird geladen…