Reaktionsgleichung
[N:1]1([CH2:10][C:11]([N:13]([O:15][CH3:16])[CH3:14])=[O:12])[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[N:2]1.C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[Cl:27][C:28]1[CH:35]=[CH:34][C:31]([CH2:32]Br)=[CH:30][CH:29]=1>C1COCC1>[N:1]1([CH:10]([CH2:32][C:31]2[CH:34]=[CH:35][C:28]([Cl:27])=[CH:29][CH:30]=2)[C:11]([N:13]([O:15][CH3:16])[CH3:14])=[O:12])[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[N:2]1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 2.0 g (9 mmol) of 2-(1H-1,2,3-benzotriazol-1-yl)-N-methoxy-N-methylacetamide in 15 mL anhydrous THF at −78° C., 10 mL (10 mmol) of 1M lithium bis(trimethylsilyl)amide was added dropwise. After stirring for 25 min, a solution of 2.06 g (10 mmol) of 4-chlorobenzyl bromide in 2 mL anhydrous THF was added. The resulting reaction mixture was allowed to warm to RT and stirred for 6 h. This reaction was quenched, diluted with 75 mL EtOAc and washed 3 times with 10 mL each of brine, After drying the organic phase solvent removal afforded a crude product which was purified on silica gel using 40% EtOAc in hexane as solvent to afford the desired product as a solid. 1H NMR: (CDCl3): δ 3.2 (s, 3H), 3.34 (s, 3H), 3.52 (m, 1H), 3.7 (m, 1H), 6.32 (t, 1H), 6.9-8.2 (m, 8H).
Aufarbeitung
- customThe resulting reaction mixture
- stirringstirred for 6 h
- customThis reaction was quenched
- additiondiluted with 75 mL EtOAc
- washwashed 3 times with 10 mL each of brine
- customAfter drying
- customthe organic phase solvent removal
- customafforded a crude product which
- customwas purified on silica gel using 40% EtOAc in hexane as solvent
Quellen und Nachweise
- ORD-Eintrag
- ord-5cd5b028df3246528087d6b0b126e15f
- Quelldatensatz
- uspto-grants-2008_09
- Patentnummer
- US07423067B2
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