Reaktionsgleichung
[C:1]([C:5]1[CH:6]=[C:7]([C:19](=[O:21])[CH3:20])[CH:8]=[C:9]([O:11][CH:12]([CH2:16][O:17][CH3:18])[CH2:13][O:14][CH3:15])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[Br-:22].[Br-].[Br-].C1([N+](C)(C)C)C=CC=CC=1.C1([N+](C)(C)C)C=CC=CC=1.C1([N+](C)(C)C)C=CC=CC=1>CO.C1COCC1.C(Cl)Cl>[Br:22][CH2:20][C:19]([C:7]1[CH:8]=[C:9]([O:11][CH:12]([CH2:16][O:17][CH3:18])[CH2:13][O:14][CH3:15])[CH:10]=[C:5]([C:1]([CH3:4])([CH3:2])[CH3:3])[CH:6]=1)=[O:21]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
1-[3-tert-Butyl-5-(2-methoxy-1-methoxymethylethoxy)phenyl]ethanone (O2.072; 1.64 g) was dissolved in methanol/THF (30/30 ml) and admixed while stirring with phenyltrimethylammonium tribromide (2.09 g). The mixture was stirred at RT for 1 h, then diluted with DCM and washed once with 5% sodium thiosulfate solution. The DCM phase was dried over magnesium sulfate, filtered and concentrated. The residue was purified using silica gel (80 g cartridge, n-heptane/MtB ether gradient of 0-30% within 60 min). 890 mg of the title compound were obtained.
Aufarbeitung
- washwashed once with 5% sodium thiosulfate solution
- dry with materialThe DCM phase was dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified
- customsilica gel (80 g cartridge, n-heptane/MtB ether gradient of 0-30% within 60 min)
Quellen und Nachweise
- ORD-Eintrag
- ord-376b57f13eb943a7b2942a8293aac9a9
- Quelldatensatz
- uspto-grants-2011_12
- Patentnummer
- US08076336B2
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