Reaktion #5141

ord-d9b4a74b6f174994bb36ba06d02ba840

Reaktionsgleichung

C[Si](C)(C)Cl
chlorotrimethylsilane
Cc1ccc(C)c(Br)c1
2-bromo-p-xylene
CCCCCC.[Li][CH2]CCC
n-butyllithium hexane
Cc1ccc(C)c([Si](C)(C)C)c1
2-Trimethylsilyl-p-xylene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was removed under reduced pressure
  2. 2
    workup.DISTILLATIONthe residne was redistilled in vacuo
  3. 3
    Sonstigeto afford titled compound(TSTX) in colorloss state

Vorschrift

To a stirred solution of 1.0M of 2-bromo-p-xylene in diethyl ether at 0° C. was added n-butyllithium hexane solution solwly, and the mixture was stirrd for 5 hr. To the above reaction mixture was added 1.0M of chlorotrimethylsilane as dropwise and it was stirred for 24 hr. The solvent was removed under reduced pressure, and the residne was redistilled in vacuo to afford titled compound(TSTX) in colorloss state. The structure of product was identified by infrared and nuclear magnetic resonance spectrum, and the result is summarized in Table 1.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05243010uspto-grants-1993_09