Hydrochloric Acid → 1-Chlorononan-4-one

HRID 973332

Reaktionsgleichung

Reaktionsgleichung von HRID 973332
[CH2:1](Br)[CH2:2][CH2:3][CH2:4][CH3:5].[Mg].[Cl:8][CH2:9][CH2:10][CH2:11][C:12]#N.Cl.CC[O:17]CC>>[Cl:8][CH2:9][CH2:10][CH2:11][C:12](=[O:17])[CH2:1][CH2:2][CH2:3][CH2:4][CH3:5]

Komponenten

6

Versuchsvorschrift

To the Grignard reagent prepared from a mixture of amyl bromide (226.59 g.; 1.5 moles) and magnesium (36.48 g.; 1.5 moles) in ether (1000 ml.) is added, dropwise, during one hour, 4-chlorobutyronitrile (155.34 g.; 1.5 moles). Stirring is continued for an additional one hour. The reaction mixture is poured into a mixture of finely crushed ice (1000 g.) and concentrated hydrochloric acid (750 ml.). The ether layer is separated quickly and discarded. The aqueous layer is heated on a steam bath for one hour to hydrolyze the intermediate imine and cause the separation of the ketone as an oil. After cooling, the oil is extracted with ether and the combined extracts are washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent is removed under vacuum and the residual oil is distilled to give 69.0 g. (26%) of colorless oil, b.p. 115°-117°/14 mm.; pmr (CDCl3) δ 0.90 (3H,t), 3.56 (2H,t,CH2Cl).

Aufarbeitung

  1. additionis added
  2. waitis continued for an additional one hour
  3. customThe ether layer is separated quickly
  4. temperatureThe aqueous layer is heated on a steam bath for one hour
  5. customthe separation of the ketone as an oil
  6. temperatureAfter cooling
  7. extractionthe oil is extracted with ether
  8. washthe combined extracts are washed with saturated sodium chloride solution
  9. dry with materialdried over anhydrous sodium sulfate
  10. customThe solvent is removed under vacuum
  11. distillationthe residual oil is distilled
  12. customto give 69.0 g

Quellen und Nachweise

ORD-Eintrag
ord-e8baa329df764d49861decd282eaa274
Quelldatensatz
uspto-grants-1977_10
Patentnummer
US04055597

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