Hydrochloric Acid → (4aS,7aR)-rel-Octahydropyrrolo[3,4-b][1,4]oxazine dihydrochloride
Reaktionsgleichung
C([N:8]1[C@@H:16]2[C@@H:12]([CH2:13][NH:14][CH2:15]2)[O:11][CH2:10][CH2:9]1)C1C=CC=CC=1.[ClH:17]>C(O)C.[Pd]>[ClH:17].[ClH:17].[C@@H:12]12[CH2:13][NH:14][CH2:15][C@@H:16]1[NH:8][CH2:9][CH2:10][O:11]2Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
26 g (0.11 mol, 92% strength) of cis-5-benzyl-2-oxa-5,8-diazabicyclo[4.3.0]nonane are hydrogenated on 3 g of palladium/active charcoal (10% Pd) at 100° C. and 100 bar H2 in 180 ml of ethanol and 19 ml of concentrated hydrochloric acid. The catalyst is filtered off with suction, the filtrate is concentrated and the crystals which have separated out are dried in a desiccator over phosphorus pentoxide.
Aufarbeitung
- filtrationThe catalyst is filtered off with suction
- concentrationthe filtrate is concentrated
- customthe crystals which have separated out
- dry with materialare dried in a desiccator over phosphorus pentoxide
Quellen und Nachweise
- ORD-Eintrag
- ord-ccf30365f6c34b6d8d579e5f4381522a
- Quelldatensatz
- uspto-grants-1996_01
- Patentnummer
- US05480879
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