Reaktion #3999

ord-c8ad3021517e47849a4ef0618fa4b5f1

Reaktionsgleichung

CC(C)=O.O=C=O
dry ice acetone
FC(F)(F)C(c1ccc(Br)cc1)(c1ccc(Br)cc1)C(F)(F)F
2,2-bis(4-bromophenyl)hexafluoropropane
[Li][CH2]CCC
n-butyllithium
C[Si](C)(C)Cl
chlorotrimethylsilane
C[Si](C)(C)c1ccc(C(c2ccc([Si](C)(C)C)cc2)(C(F)(F)F)C(F)(F)F)cc1
2,2-bis(4-trimethylsilylphenyl)hexafluoropropane

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas then made to the reaction mixture at -78° C
  2. 2
    WaschenThe organic layer was washed with 2×150 ml saturated sodium chloride solution and 2×150 ml water
  3. 3
    SonstigeThe organic layer was dried
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated

Vorschrift

To a solution of 4.62 g (0.1 mole) 2,2-bis(4-bromophenyl)hexafluoropropane in 75 ml of anhydrous tetrahydrofuran was added dropwise 28 ml (0.4 moles) of a 1.4 molar solution of n-butyllithium in hexane while the reaction mixture was cooled in a dry ice-acetone slush. The reaction mixture was stirred for one half hour at -78° C. A dropwise addition of chlorotrimethylsilane (5 ml, 0.04 moles) was then made to the reaction mixture at -78° C. The stirring slurry was allowed to come to ambient temperature over 16 hours. To the reaction mixture was added 100 ml hexane. The organic layer was washed with 2×150 ml saturated sodium chloride solution and 2×150 ml water. The organic layer was dried, filtered, and concentrated to yield the white crystalline product 2,2-bis(4-trimethylsilylphenyl)hexafluoropropane.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04722985uspto-grants-1988_02