Diethylaluminum chloride → HCID 16689304, Verbindung

HRID 1293491

Reaktionsgleichung

Reaktionsgleichung von HRID 1293491
[Al:1](Cl)([CH2:4][CH3:5])[CH2:2][CH3:3].[CH2:7]([O:9][C:10]1([Li])[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=[CH:12][CH2:11]1)[CH3:8].C([Li])(C)(C)C.C(OC1C2C(=CC=CC=2)C=CC=1)C>CCCCCC.C(OCC)C>[CH2:7]([O:9][C:10]1[CH:11]=[CH:12][CH:13]=[C:14]2[C:19]=1[C:18]([Al:1]([CH2:4][CH3:5])[CH2:2][CH3:3])=[CH:17][CH:16]=[CH:15]2)[CH3:8]

Komponenten

7

Versuchsvorschrift

2.5 ml (20 mmol) of Et2AlCl are added dropwise at −40° C. to a suspension of 50 ml of diethyl ether and 3.5 g (20 mmol) of (1-ethoxynaphth-1-yl)lithium, prepared from 33 ml (56 mmol) of t-butyllithium (1.7M solution in pentane) and 9.7 g (56 mmol) of 1-ethoxynaphthalene in 200 ml of hexane. The mixture is slowly brought to room temperature and stirred at room temperature for 24 h. The mixture is subsequently decanted off from the solid, the solvent is removed, the residue is taken up in 35 ml of toluene and filtered through a D4 frit. After removal of the toluene, fractional distillation gives (8-ethoxynaphth-1-yl)diethylaluminium as pale-yellow liquid having a boiling point of 146° C. at 0.01 mbar.

Aufarbeitung

  1. customis slowly brought to room temperature
  2. customThe mixture is subsequently decanted off from the solid
  3. customthe solvent is removed
  4. filtrationfiltered through a D4 frit
  5. customAfter removal of the toluene, fractional distillation

Quellen und Nachweise

ORD-Eintrag
ord-f1f64abcf1c44fc987c528aa90604857
Quelldatensatz
uspto-grants-2007_07
Patentnummer
US07238757B2

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