Reaktionsgleichung
[CH3:1][C:2]1([CH3:15])[S:6][C@@H:5]2[C:7]([Br:11])([Br:10])[C:8](=[O:9])[N:4]2[C@H:3]1[C:12]([OH:14])=[O:13]>[Pd].[Pd].C([O-])([O-])=O.[Ca+2]>[CH3:1][C:2]1([CH3:15])[S:6][C@@H:5]2[C:7]([Br:11])([Br:10])[C:8](=[O:9])[N:4]2[C@H:3]1[C:12]([OH:14])=[O:13].[CH3:1][C:2]1([CH3:15])[S:6][C@@H:5]2[CH2:7][C:8](=[O:9])[N:4]2[C@H:3]1[C:12]([OH:14])=[O:13]Komponenten
5
Edukt 1
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Pratt, U.S. Pat. No. 4,180,506, describes catalytic hydrogenation of 6,6-dibromopenicillanic acid over Pd/C catalyst to produce a mixture of 6-alpha- and 6-beta-bromopenicillanic acid. Clayton, J. Chem. Soc. (C), pp. 2123-2127 (1969), describes the hydrogenation of methyl 6,6-dibromopenicillanate over Pd/CaCO3 to produce methyl 6-alpha-bromopenicillanate and methyl penicillanate; and hydrogenation of 6,6-dibromopenicillanic acid over the same catalyst to produce penicillanic acid.
Aufarbeitung
- customto produce
- additiona mixture of 6-alpha- and 6-beta-bromopenicillanic acid
- customto produce methyl 6-alpha-bromopenicillanate and methyl penicillanate
Quellen und Nachweise
- ORD-Eintrag
- ord-433695d9204e48309c42fc99dc140bbc
- Quelldatensatz
- uspto-grants-1984_08
- Patentnummer
- US04468351
Verknüpfte Notizen
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