Hydrochloric Acid → 1-Chlorononan-4-one

HRID 2083275Notes

Reaction equation

HRID 2083275 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 mols) 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 (750 ml.). The ether layer is separated quickly and discarded. The aqueous layer is heated on a stream 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).

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 stream 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-8af7785f15634df99429a04f781cf201
Source dataset
uspto-grants-1978_04
Patent number
US04085125

Reaction notes

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