Reaktionsgleichung
Br[C:2]1[CH2:6][CH2:5][CH2:4][C:3]=1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH3:13][S:14][C:15]1[CH:20]=[CH:19][C:18](B(O)O)=[CH:17][CH:16]=1>>[C:7]1([C:3]2[CH2:4][CH2:5][CH2:6][C:2]=2[C:18]2[CH:19]=[CH:20][C:15]([S:14][CH3:13])=[CH:16][CH:17]=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1Komponenten
3
Versuchsvorschrift
Following a synthetic procedure which was similar to the one outlined in Step 3 of Example 1, 750 mg (3.4 mmol) of 1-bromo-2-phenylcyclopentene (Step 1) was reacted with 1.2 g (6.8 mmol) of 4-methylthiophenylboronic acid (Example 1, Step 1). Purification by silica gel chromatography (MPLC) with hexane gave 800 mg (89%) of 1-(2-phenylcyclopenten-1-yl) -4-(methylthio)benzene as an oil: NMR (CDCl3) d 2.00-2.17 (m, 2H), 2.46 (s, 3H) , 2.86-3.01 (m, 4H) , 7.08-7.19 (m, 4H) , 7.19-7.32 (m, 5H) .
Aufarbeitung
- customPurification by silica gel chromatography (MPLC) with hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-9a54f5bfd5f445c796cc0b47a204e068
- Quelldatensatz
- uspto-grants-1994_09
- Patentnummer
- US05344991
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