Reaktionsgleichung
Br[C:2]1[C:3]2[C:8]([CH:9]=[C:10]3[C:15]=1[CH:14]=[CH:13][CH:12]=[CH:11]3)=[CH:7][CH:6]=[CH:5][CH:4]=2.BrC1C=CC=CC=1O>CCOCC.CCCCCC.[Cl-].[Cl-].[Zn+2].CC(C)([P](C(C)(C)C)([Pd][P](C(C)(C)C)(C(C)(C)C)C(C)(C)C)C(C)(C)C)C>[CH:4]1[C:3]2[C:8](=[CH:9][C:10]3[C:15]([CH:2]=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH:7]=[CH:6][CH:5]=1Komponenten
Reagenzien, Katalysatoren, Lösungsmittel 4
Reaktionsbedingungen
- Temperatur
- -30 °C
Versuchsvorschrift
A solution of 9-bromoanthracene (0.67 g, 2.6 mmol, 1.2 eq) in dry Et2O (13 mL) under N2 was cooled to −30° C. and nBuli (1.6 M in hexane, 1.6 mL, 2.6 mmol, 1.2 eq) was added dropwise. The solution was stirred for 20 min. at −30° C. followed by dropwise addition of ZnCl2 (0.50 M in THF, 5.2 mL, 2.6 mmol, 1.2 eq). The reaction was stirred and warmed to RT over 30 min. The volatiles were removed under N2 purge and the residue was redissolved in 3:1 THF/NMP (11 mL). The MOM-protected bromophenol (2.2 mmol, 1.0 eq) and Pd(PtBu3)2 (22 mg, 44 μmol, 4 mol %) were added and the reaction was heated to 100° C. for 2 h. The reaction was cooled to RT and the THF was removed. The residue was diluted with CH2Cl2, washed with 1 M HCl, and dried over Na2SO4. The crude material was purified by flash chromatography.
Aufarbeitung
- stirringThe reaction was stirred
- temperaturewarmed to RT over 30 min
- customThe volatiles were removed under N2
- custompurge
- dissolutionthe residue was redissolved in 3:1 THF/NMP (11 mL)
- temperaturethe reaction was heated to 100° C. for 2 h
- temperatureThe reaction was cooled to RT
- customthe THF was removed
- additionThe residue was diluted with CH2Cl2
- washwashed with 1 M HCl
- dry with materialdried over Na2SO4
- customThe crude material was purified by flash chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-2b9cd45206bd483889c44f0a2aa70c02
- Quelldatensatz
- uspto-grants-2006_08
- Patentnummer
- US07091292B2
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