Ammonium Chloride → HCID 19039134, Verbindung
Reaktionsgleichung
O1CCCC1.C1(C)C=CC=CC=1.[Cl-].[F:14][C:15]1[CH:20]=[CH:19][C:18]([Zn+])=[CH:17][CH:16]=1.I[C:23]1[CH:28]=[CH:27][C:26]([CH:29]2[CH2:34][CH2:33][Si:32]([C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=3)([CH2:35][CH2:36][CH3:37])[CH2:31][CH2:30]2)=[CH:25][CH:24]=1.[Cl-].[NH4+]>[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(OCC)(=O)C.O1CCCC1>[F:14][C:15]1[CH:20]=[CH:19][C:18]([C:23]2[CH:24]=[CH:25][C:26]([CH:29]3[CH2:30][CH2:31][Si:32]([C:38]4[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=4)([CH2:35][CH2:36][CH3:37])[CH2:33][CH2:34]3)=[CH:27][CH:28]=2)=[CH:17][CH:16]=1Komponenten
8
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
A 15 ml tetrahydrofuran-toluene (1:1) solution of 1.0M 4-fluorophenyl zinc chloride was dripped into a mixture of 4.20 g of 4-(4-iodophenyl)-1-phenyl-1-n-propyl-1-silacyclohexane, 30 mg of tetrakis (triphenylphosphine) palladium(0) and 30 ml of tetrahydrofuran. After stirring for 8 hours at room temperature, the mixture was poured into a saturated aqueous solution of ammonium chloride and extraction was conducted using ethyl acetate. Using conventional washing, drying and concentration processes, 4-(4-(4-fluorophenyl)phenyl)-1-phenyl-1-n-propyl-1-silacyclohexane was obtained.
Aufarbeitung
- customdrying
- concentrationconcentration processes
Quellen und Nachweise
- ORD-Eintrag
- ord-8184705a7ada4a6d8a814fefff2fed8d
- Quelldatensatz
- uspto-grants-1997_06
- Patentnummer
- US05641431
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