Sulfuric Acid → 1,4-Dibromo-2,2-diethoxy-3-butanone

HRID 280731

Reaktionsgleichung

Reaktionsgleichung von HRID 280731
[Br:1][CH2:2][C:3](=[O:8])[C:4](=[O:7])[CH2:5][Br:6].[CH2:9]([O:11]C(OCC)OCC)[CH3:10].S(=O)(=O)(O)O.[CH3:24][CH2:25]CCCC>C(Cl)(Cl)Cl>[Br:1][CH2:2][C:3]([O:11][CH2:9][CH3:10])([O:8][CH2:24][CH3:25])[C:4](=[O:7])[CH2:5][Br:6]

Komponenten

6

Versuchsvorschrift

A mixture of 40 g (0.164 mol) of 1,4-dibromo 2,3-butanedione, 60 ml (0.36 M) of triethylorthoformate, and 2 ml of concentrated sulfuric acid was stirred at room temperature for 14 hours, then diluted with 600 ml of chloroform, and washed successively with 100 ml portions of water, 0.5 N hydrochloric acid and saturated sodium chloride solution. The organic solution was dried over anhydrous sodium sulfate filtered, and evaporated leaving an oil. The oil was taken up into 300 ml of hexane and filtered to remove some insoluble material. The hexane filtrate was cooled in a dry-ice/acetone bath, and the resulting precipitate was collected by filtration and dried to give 44 g (84%) of 1,4-dibromo-2,2-diethoxy-3-butanone as a white crystalline solid, mp 40°-41.5°; nmr (CDCl3) (δ): 4.50 (s, 2H); 3.6-3.2 (m, 6H); 1.22 (t, 6H).

Aufarbeitung

  1. washwashed successively with 100 ml portions of water, 0.5 N hydrochloric acid and saturated sodium chloride solution
  2. dry with materialThe organic solution was dried over anhydrous sodium sulfate
  3. filtrationfiltered
  4. customevaporated
  5. customleaving an oil
  6. filtrationfiltered
  7. customto remove some insoluble material
  8. temperatureThe hexane filtrate was cooled in a dry-ice/acetone bath
  9. filtrationthe resulting precipitate was collected by filtration
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-21e8fdd272e54135b25045c62ac914af
Quelldatensatz
uspto-grants-1986_05
Patentnummer
US04590299

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