Reaktionsgleichung
C[CH:2]1[C:9](=[O:10])[C:5]2S[CH:7]=[CH:8][C:4]=2[CH2:3]1.Br[C:12]1[C:17](C)=[CH:16][CH:15]=[CH:14][C:13]=1[CH2:19]Br.Br[C:22]1[C:27]([CH3:28])=[CH:26][CH:25]=[CH:24][C:23]=1C.Cl[Pd:31]Cl>O1CCCC1>[CH:22]1[CH:23]=[CH:24][C:8](/[CH:4]=[CH:5]/[C:9](/[CH:2]=[CH:3]/[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[O:10])=[CH:7][CH:27]=1.[CH:24]1[CH:25]=[CH:26][C:27](/[CH:28]=[CH:5]/[C:9](/[CH:2]=[CH:19]/[C:13]2[CH:12]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[O:10])=[CH:22][CH:23]=1.[Pd:31]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
All manipulations with air and moisture sensitive compounds were performed either in an atmosphere of thoroughly purified argon using a standard Schlenk technique or in a controlled atmosphere Glove Box (Vacuum Atmospheres Co.). Tetrahydrofuran (THF, Merck=Merck KGaA, Darmstadt, Germany) and diethyl ether (Merck) for synthesis were purified by distillation over LiAlH4, and stored over sodium benzophenone ketyl under an inert atmosphere; prior to use, the solvents were distilled from the benzophenone ketyl. Hydrocarbon solvents such as benzene (Merck), toluene (Merck) and hexanes (Merck) and including benzene-d6 for NMR measurements were typically distilled over CaH2, and were stored over Na/K alloy under an inert atmosphere; prior to use, the solvents were distilled from the Na/K alloy. Methylene chloride (Merck) and CCl2D2 (Cambridge Isotope) for NMR measurements were distilled and stored over CaH2 under an inert atmosphere; prior to use, the solvents were distilled from the CaH2. Benzothiophene (Aldrich), 2.5 M nBuLi in hexanes (Acros=Acros Organics), 1.6 M MeLi in ether (Acros), 3.0 M methylzinc chloride in THF (Aldrich), 1.0 M phenylmagnesium bromide in THF (Aldrich), 1.0 M p-tolylmagnesium bromide in THF (Aldrich), 1.0 M mesityl bromide in THF (Aldrich), 0.5 M 4-N,N-dimethylaminophenylmagnesium bromide in THF (Aldrich), 2-bromobenzylbromide (Aldrich), 2-chlorobenzylchloride (Merck), diethyl methylmalonate (Acros), 2-bromobenzotrifluoride (Acros), 3-bromobenzotrifluoride (Acros), 1,3-bis(trifluoromethyl)-5-bromobenzene (Aldrich), 4-tert-butylbromobenzene (Acros), 2-bromo-4-isopropylaniline (Aldrich), 2-bromo-2-methylpropanoyl bromide (Aldrich), 1-bromonaphthalene (Acros), 0.5 M ZnCl2 in THF (Aldrich), and Pd(PtBu3)2 (Strem=Strem Chemical Co.), 2-[di(tert-butyl)phosphino]-1,1′-biphenyl (Strem), ZrCl4(THF)2 (Aldrich), NaBH4 (Acros), NaBPh4 (Aldrich), anhydrous powdered AlCl3 (Merck), and dichlorodimethylsilane (Merck) were used as obtained. Solutions of Grignard reagents (2-trifluoromethylphenylmagnesium bromide, 3-trifluoromethylphenylmagnesium bromide, 4-tert-butylphenylmagnesium bromide, 1,3-bis(trifluoromethyl)-5-bromobenzene, and 1-naphthylmagnesium bromide) in THF were obtained from magnesium turnings (Aldrich) and the respective arylbromides in THF at reflux. 5-Methyl-4,5-dihydro-6H-cyclopenta[b]-thiophen-6-one [Ryabov, A. N.; Gribkov, D. V.; Izmer, V. V.; Voskoboynikov, A. Z. Organometallics 2002, 21, 2842] was prepared according to the published method. 2-Bromo-1-(bromomethyl)-3-methylbenzene [Baker, R. W.; Foulkes, M. A.; Griggs, M.; Nguyen, B. N. Tetrahedron Lett. 2002, 43, 9319] was prepared from 2-bromo-m-xylene (Acros) according to the published procedure. Pd(dba)2 was prepared from PdCl2 (Aldrich) and dibenzolidenacetone (Acros) as described in literature [Coulson, D. R. Inorg. Synth. 1972, 13, 121].
Quellen und Nachweise
- ORD-Eintrag
- ord-1cf0ee06dd3749d99910b4ec3abd1822
- Quelldatensatz
- uspto-grants-2011_03
- Patentnummer
- US07910783B2
Verknüpfte Notizen
Wird geladen…