Hydrochloric Acid → 1-Chlorononan-4-one

HRID 328759

Reaction equation

HRID 328759 reaction equation
[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]

Participants

6

Procedure

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 (100 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 (750ml.). 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 O.90 (3H,t), 3.56 (2H,t,CH2Cl).

Workup

  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

Sources & evidence

ORD record
ord-a59fd1cdf7a24254962cf5bbc297f12b
Source dataset
uspto-grants-1977_04
Patent number
US04018802

Linked notes

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