Hydrochloric Acid → 1,2,3,4-Tetrahydrobenzo-furo[3,2-c]pyridine hydrochloride
Reaktionsgleichung
[ClH:1].[C:2]1([O:8]N)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[NH:11]1[CH2:16][CH2:15][C:14](O)(O)[CH2:13][CH2:12]1.Cl>CC(O)C>[ClH:1].[CH2:12]1[C:13]2[C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[O:8][C:14]=2[CH2:15][CH2:16][NH:11]1Komponenten
Reaktionsbedingungen
- Temperatur
- 20 °C
Versuchsvorschrift
A mixture of O-phenylhydroxylamine hydrochloride (1:1) (0.625 mol) and 4,4-piperidinediol hydrochloride (1:1) (0.682 mol) in 2-propanol (615 ml) was stirred at 20° C. HCl (353 ml) was added dropwise at 20 ° C. The reaction mixture was gently heated to reflux temperature. The reaction mixture was stirred and refluxed for 3 hours, then cooled to room temperature. The precipitate was filtered off, washed with diisopropyl ether, and dried. This fraction was crystallized from water (1600 ml). The desired compound was allowed to crystallize out while stirring. The precipitate was filtered off, washed with 2-propanol and diisopropyl ether, then dried, yielding 84 g (64%) of 1,2,3,4-tetrahydrobenzo-furo[3,2-c]pyridine hydrochloride (1:1) (interm. 1).
Aufarbeitung
- temperatureThe reaction mixture was gently heated
- temperatureto reflux temperature
- stirringThe reaction mixture was stirred
- temperaturerefluxed for 3 hours
- temperaturecooled to room temperature
- filtrationThe precipitate was filtered off
- washwashed with diisopropyl ether
- customdried
- customThis fraction was crystallized from water (1600 ml)
- customto crystallize out
- stirringwhile stirring
- filtrationThe precipitate was filtered off
- washwashed with 2-propanol and diisopropyl ether
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-78dcf7c3f9c04c82b22c8e4610fa32c3
- Quelldatensatz
- uspto-grants-2002_03
- Patentnummer
- US06352999B1
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