Reaktionsgleichung
[Br:1][CH2:2][CH:3]([OH:27])[CH2:4][O:5][C:6]1[C:14]([Br:15])=[C:13]2[C:9]([CH:10]=[N:11][N:12]2[CH2:16][C@@H:17]([O:19][Si:20]([C:23]([CH3:26])([CH3:25])[CH3:24])([CH3:22])[CH3:21])[CH3:18])=[CH:8][CH:7]=1.[CH:28]([O:30][CH2:31][CH3:32])=[CH2:29]>ClCCl.C1(C)C=CC(S(O)(=O)=O)=CC=1>[Br:15][C:14]1[C:6]([O:5][CH2:4][CH:3]([O:27][CH:28]([O:30][CH2:31][CH3:32])[CH3:29])[CH2:2][Br:1])=[CH:7][CH:8]=[C:9]2[C:13]=1[N:12]([CH2:16][C@@H:17]([O:19][Si:20]([C:23]([CH3:26])([CH3:25])[CH3:24])([CH3:21])[CH3:22])[CH3:18])[N:11]=[CH:10]2Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a solution of the product from Step E (1.85 g, 3.54 mmol) and p-toluenesulfonic acid (0.01 g) in dichloromethane (50 mL) at 0° C. was added ethyl vinyl ether (1 mL, 10.5 mmol). After 30 min the reaction was quenched with a saturated solution of sodium bicarbonate (50 mL) and extracted with EtOAc (3×80 mL). Evaporation and purification by chromatography (silica, 1% to 8% EtOAc/hexane) gave a viscous oil (1.79 g, 81%): LC/MS (+APCI) m/z 595 (M+H).
Aufarbeitung
- customAfter 30 min the reaction was quenched with a saturated solution of sodium bicarbonate (50 mL)
- extractionextracted with EtOAc (3×80 mL)
- customEvaporation and purification by chromatography (silica, 1% to 8% EtOAc/hexane)
Quellen und Nachweise
- ORD-Eintrag
- ord-5db1d6e901934fd2839379fc377ad21a
- Quelldatensatz
- uspto-grants-2005_04
- Patentnummer
- US06881749B2
Verknüpfte Notizen
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