Mannitol → 2,5-anhydro-1-deoxy-1-(diethoxyphosphinyl)-1-fluoro-D-mannitol
Reaktionsgleichung
C(O)[C@@H]([C@H]([C@@H]([C@@H](CO)O)O)O)O.[CH2:13]([O:15][P:16]([O:43][CH2:44][CH3:45])([CH:18]([F:42])[C@@H:19]1[O:39][C@H:38]([CH2:40][OH:41])[C@@H:29]([O:30]CC2C=CC=CC=2)[C@@H:20]1[O:21]CC1C=CC=CC=1)=[O:17])[CH3:14].C(O)[C@H]([C@H]([C@@H]([C@@H](CO)O)O)O)O.P([O-])(OC1C=CC=CC=1)(OC1C=CC=CC=1)=O.[H][H]>CO.[OH-].[Pd+2].[OH-]>[CH2:13]([O:15][P:16]([O:43][CH2:44][CH3:45])([CH:18]([F:42])[C@H:19]1[O:39][C@H:38]([CH2:40][OH:41])[C@@H:29]([OH:30])[C@@H:20]1[OH:21])=[O:17])[CH3:14]Komponenten
7
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of 330 mg of 2,5-anhydro-1-deoxy-1-(diethoxyphosphinyl)-1-fluoro-3,4-bis-O-(phenylmethyl)-D-glucitol D-glucitol and D-mannitol, diphenyl phosphate mixture in 20 ml of methanol was hydrogenated over palladium hydroxide catalyst until hydrogen uptake ceased. Filtration and removal of the solvent gave a yellow oil. This oil was purified by flash chromatography taking 20 ml fractions Fractions 1-26 were eluted with 3% methanol in dichloromethane and after evaporation gave 135 mg of 2,5-anhydro-1-deoxy-1-(diethoxyphosphinyl)-1-fluoro-D-mannitol, 6-(diphenyl phosphate).
Aufarbeitung
- filtrationFiltration and removal of the solvent
- customgave a yellow oil
- customThis oil was purified by flash chromatography
- washwere eluted with 3% methanol in dichloromethane
- customafter evaporation
Quellen und Nachweise
- ORD-Eintrag
- ord-b9c24b1e61e84ceab1c0c72a804821e8
- Quelldatensatz
- uspto-grants-1990_07
- Patentnummer
- US04943629
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