Potassium Hydroxide → 3-Bromostyrene

HRID 263825

Reaktionsgleichung

Reaktionsgleichung von HRID 263825
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([C:8]#[C:9][Si](C)(C)C)[CH:3]=1.[OH-].[K+]>CO.O>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH:8]=[CH2:9])[CH:3]=1

Komponenten

5

Versuchsvorschrift

To a solution of 1-bromo-3-trimethylsilylethynylbenzene (20.5 g, 81.0 mmol) in degassed methanol (500 ml), there was added potassium hydroxide (31 mg, 0.55 mmol) in water (1 ml). The solution was stirred at room temperature until G.C. analysis indicated the reaction was complete (5.0 h). The reaction mixture was diluted with an equal volume of water, and extracted with n-pentane (5×500 ml). The combined organic layers were dried (MgSO4) and the solvent removed under reduced pressure to yield a yellow liquid. The liquid was distilled via bulb-to-bulb vacuum distillation to yield the product (1c) (13.0 g, 90%) as a clear liquid: bp 40° CC/1 torr; 1H NMR (200 MHz, CDCl3) c3.35(s), 7.23(t), 7.40(m), 7.65(t).

Aufarbeitung

  1. custom(5.0 h)
  2. extractionextracted with n-pentane (5×500 ml)
  3. dry with materialThe combined organic layers were dried (MgSO4)
  4. customthe solvent removed under reduced pressure
  5. customto yield a yellow liquid
  6. distillationThe liquid was distilled via bulb-to-bulb vacuum distillation

Quellen und Nachweise

ORD-Eintrag
ord-f754b98a0a84441e98bc3a836e2762b3
Quelldatensatz
uspto-grants-1997_07
Patentnummer
US05645809

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