Hydrochloric Acid → (R)-8-Fluoro-5-hydroxy-3-(N-3-pentyl-N-n-propylamino)chroman hydrochloride
Reaktionsgleichung
[F:1][C:2]1[CH:3]=[CH:4][C:5]([OH:21])=[C:6]2[C:11]=1[O:10][CH2:9][C@H:8]([N:12]([CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH2:13][CH2:14][CH3:15])[CH2:7]2.[ClH:22]>CCOCC>[ClH:22].[F:1][C:2]1[CH:3]=[CH:4][C:5]([OH:21])=[C:6]2[C:11]=1[O:10][CH2:9][C@H:8]([N:12]([CH:16]([CH2:17][CH3:18])[CH2:19][CH3:20])[CH2:13][CH2:14][CH3:15])[CH2:7]2Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
(R)-8-Fluoro-5-hydroxy-3-(N-3-pentyl-N-n-propylamino)chroman (180 mg, 0.6 mmol) was dissolved in ether. HCl in ether was added to precipitate the HCl-salt, and gave after drying 200 mg of (R)-8-fluoro-5-hydroxy-3-(N-3-pentyl-N-n-propylamino)chroman hydrochloride as a white powder. Mp: 80°-100° C. (sinters).
Aufarbeitung
- customto precipitate the HCl-salt
- customgave
- dry with materialafter drying 200 mg of (R)-8-fluoro-5-hydroxy-3-(N-3-pentyl-N-n-propylamino)chroman hydrochloride as a white powder
Quellen und Nachweise
- ORD-Eintrag
- ord-215a6116fcb24d3585b3b07dd2228a4f
- Quelldatensatz
- uspto-grants-1997_07
- Patentnummer
- US05650524
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