Trifluoroacetic acid → 4-Octyl-2'-fluoro-4'-bromobiphenyl

HRID 1769565Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1769565
[C:1]([C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:21]=[CH:20][C:19]([Br:22])=[CH:18][C:17]=2[F:23])=[CH:12][CH:11]=1)(=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].FC(F)(F)C(O)=O.C([SiH](CC)CC)C>O>[CH2:1]([C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:21]=[CH:20][C:19]([Br:22])=[CH:18][C:17]=2[F:23])=[CH:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]

Komponenten

5

Versuchsvorschrift

A reaction vessel was charged with 3.75 g of 4-octanoyl-2'-fluoro-4'-bromobiphenyl and 20 ml of trifluoroacetic acid. To the mixture was added dropwise 2.4 g of triethylsilane with stirring at room temperature. After stirring for 6 hours, the reaction liquid was poured into water and the mixture was extracted with benzene. The benzene extract was washed successively with water, an aqueous solution of sodium hydrogen carbonate and water, and then dried over Glauber's salt. The solvents were distilled off and the residue was distilled in a glass tube oven (GTO) to obtain 2.56 g (71.1%) of 4-octyl-2'-fluoro-4'-bromobiphenyl. GTO-set temperature: 150° C./0.2 mmHg.

Aufarbeitung

  1. stirringAfter stirring for 6 hours
  2. customthe reaction liquid
  3. extractionthe mixture was extracted with benzene
  4. extractionThe benzene extract
  5. washwas washed successively with water
  6. dry with materialan aqueous solution of sodium hydrogen carbonate and water, and then dried over Glauber's salt
  7. distillationThe solvents were distilled off
  8. distillationthe residue was distilled in a glass tube oven (GTO)

Quellen und Nachweise

ORD-Eintrag
ord-2782fb43374f41399aaaf810bc2ad426
Quelldatensatz
uspto-grants-1995_01
Patentnummer
US05382380

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