Chlorotrimethylsilane → HCID 18670031, Verbindung

HRID 1004854Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1004854
[CH:1]1([C:10]([CH:13]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14]2)([CH3:12])[CH3:11])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.C([Li])CCC.C1(C(C2C3C(=CC=CC=3)C=C2)(C)C)C2C(=CC=CC=2)C=C1.[Li].[Li].[Si:50](Cl)([CH3:53])([CH3:52])[CH3:51]>CCOCC.CCCCC>[CH3:51][Si:50]([CH3:53])([CH3:52])[C:15]1[C:16]2[C:21](=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:13]([C:10]([CH:1]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[C:3]([Si:50]([CH3:53])([CH3:52])[CH3:51])=[CH:2]2)([CH3:11])[CH3:12])[CH:14]=1

Komponenten

7

Edukt 4

HCID 6397ChlorotrimethylsilaneHCID 117806711H-Indene, (1-methylethylidene)bis-HCID 69536615HCID 69536615, VerbindungHCID 178418339Butyllithium

Produkt 1

HCID 18670031HCID 18670031, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283Diethyl EtherLösungsmittel2×HCID 8003PentaneLösungsmittel

Versuchsvorschrift

5.45 g (20 mmol) of 2,2-bis(indenyl)propane was dissolved in 100 ml of ether. The solution thus obtained was taken to -20° C., and 22 ml of a 2.0 M solution of n-butyl-lithium in pentane was added, thus giving a suspension of dilithium-2,2-(indenyl)propane. 8.77 g (30.85 mmol) of dilithium 2,2-bis(indenyl)propane was dissolved in 100 ml of ether, and 10 ml of Me3SiCl (excess) was added at a temperature of -40° C. The resulting mixture was allowed to return to room temperature. The organic phase was then separated off, the solvent removed and the product dried in vacuo.

Aufarbeitung

  1. customThe solution thus obtained
  2. customwas taken to -20° C.
  3. customthus giving
  4. customto return to room temperature
  5. customThe organic phase was then separated off
  6. customthe solvent removed
  7. customthe product dried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-5d87ddfe82c7409db10da039d511a4f7
Quelldatensatz
uspto-grants-2000_04
Patentnummer
US06051728

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