Nonanoyl chloride → 1-(Trimethylsilyl)undec-1-yn-3-one

HRID 1073568Notes

Reaction equation

HRID 1073568 reaction equation
[C:1](Cl)(=[O:10])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9].[CH3:12][Si:13]([C:16]#[C:17][Si](C)(C)C)([CH3:15])[CH3:14].[Al+3].[Cl-].[Cl-].[Cl-]>C(Cl)Cl>[CH3:12][Si:13]([CH3:15])([CH3:14])[C:16]#[C:17][C:1](=[O:10])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9]

Participants

5

Procedure

To 500 ml of CH2Cl2 was added 53 ml (294 mmol) of nonanoyl chloride and 50 g (293.4 mmol) of bis(trimethylsilyl)acetylene. The reaction mixture was cooled in an ice bath and 40 g (300 mmol) of AlCl3 was added portionwise with stirring over 1/2 hour. After stirring for an additional hour, the reaction mixture was quenched with ice. Water was added to the reaction mixture and it was extracted 3x with 200 ml aliquots of diethyl ether. The combined extracts were washed 2x with 50 ml aliquots of saturated NaHCO3, 1 x with brine, and then dried (MgSO4). The solvent was removed in vacuo to give a brown oil which was used without further purification.

Workup

  1. temperatureThe reaction mixture was cooled in an ice bath
  2. stirringAfter stirring for an additional hour
  3. customthe reaction mixture was quenched with ice
  4. additionWater was added to the reaction mixture and it
  5. extractionwas extracted 3x with 200 ml aliquots of diethyl ether
  6. washThe combined extracts were washed 2x with 50 ml aliquots of saturated NaHCO3, 1 x with brine
  7. dry with materialdried (MgSO4)
  8. customThe solvent was removed in vacuo
  9. customto give a brown oil which
  10. customwas used without further purification

Sources & evidence

ORD record
ord-10194c0627bd4ce38236599645d39a89
Source dataset
uspto-grants-1990_11
Patent number
US04970229

Reaction notes

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