Reaktion #1435717

ord-ea8c12fb02ce482a91eeade7d48ee1e0

Reaktionsgleichung

CCCC
butane
C[Si](C)(C)OCCC1=CC=CC1
(2-trimethylsiloxy-ethyl)-cyclopentadiene
[Li][CH2]CCC
butyllithium
CCCCCC
hexane
C[Si](C)(C)OCC[c-]1cccc1.[Li+]
lithium (2-trimethylsiloxy-ethyl)-cyclopentadienide
Ausbeute 82.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONThe addition
  2. 2
    Sonstigeis realised at −78° C
  3. 3
    TemperaturIt is maintained
  4. 4
    SonstigeThen it is dried
  5. 5
    Waschenthe resulting solid washed with hexane
  6. 6
    Sonstigeleaving a powdery white solid

Vorschrift

To 7.33 g of (2-trimethylsiloxy-ethyl)-cyclopentadiene in ether, 16 ml of a 2.5 M butyllithium solution in hexane (40 mmol) is added. The addition is realised at −78° C. The immediate formation of a white solid and butane evolution are observed. It is maintained reacting for 3 hours. Then it is dried; the resulting solid washed with hexane, leaving a powdery white solid. (6.19 g, 33 mmol, Yield: 82%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07211538B2uspto-grants-2007_05