(S)-(-)-N-Boc-prolinol → tert-butyl (2S,4R)-2-formyl-4-methoxypyrrolidine-1-carboxylate
Reaktionsgleichung
[C:1]([O:5][C:6]([N:8]1[CH2:14][C@H:13]([O:15][CH3:16])[CH2:12][C@H:9]1[CH2:10][OH:11])=[O:7])([CH3:4])([CH3:3])[CH3:2].C(OC(N1CCC[C@H]1CO)=O)(C)(C)C>>[C:1]([O:5][C:6]([N:8]1[CH2:14][C@H:13]([O:15][CH3:16])[CH2:12][C@H:9]1[CH:10]=[O:11])=[O:7])([CH3:4])([CH3:3])[CH3:2]Komponenten
3
Versuchsvorschrift
With the exception that N-t-butoxycarbonyl-trans-4-methoxy-L-prolinol, instead of N-t-butoxycarbonyl-L-prolinol, was used, the same procedure as in Preparation Example 1-1 was repeated to afford the title compound. 40.8 g (97%).
Aufarbeitung
- customthe same procedure as in Preparation Example 1-1
Quellen und Nachweise
- ORD-Eintrag
- ord-d02b4517898c4804b92eb92d574988b2
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09278996B2
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