Dimethylformamide → N,N-diethyl-4-formylbenzamide

HRID 1460085Notes

Reaction equation

HRID 1460085 reaction equation
[C:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=[O:9])=[CH:6][CH:5]=1)([OH:3])=O.CN(C)C=O.S(Cl)(Cl)=O.[CH2:21]([NH:23][CH2:24][CH3:25])[CH3:22]>C(O)C.ClCCl>[CH:8]([C:7]1[CH:10]=[CH:11][C:4]([C:1]([N:23]([CH2:24][CH3:25])[CH2:21][CH3:22])=[O:3])=[CH:5][CH:6]=1)=[O:9]

Participants

7

Procedure

A mixture of 4-carboxybenzaldehyde (100 g, 0.66 mol), 1 L of dimethylformamide and 2 L of dichloromethane was cooled in an ice bath. Thionyl chloride (53 mL, 0.73 mol) was added dropwise while stirring. After 18 hours at room temperature, the mixture was cooled again and diethylamine (275 mL, 2.6 mol) was added dropwise. After stirring at room temperature for one hour the solvent was evaporated, and the residue was dissolved in aqueous 0.1M sodium hydroxide and extracted with ethyl acetate. The organic layers were washed with water and brine, dried over sodium sulfate and evaporated to give a yellow oil. Chromatography on silica gel with dichloromethane: ethanol (0-2%) gave 44.2 g (32%) of 4-formyl-N,N-diethylbenzamide as a yellow oil.

Workup

  1. temperaturewas cooled in an ice bath
  2. temperaturethe mixture was cooled again
  3. stirringAfter stirring at room temperature for one hour the solvent
  4. customwas evaporated
  5. dissolutionthe residue was dissolved in aqueous 0.1M sodium hydroxide
  6. extractionextracted with ethyl acetate
  7. washThe organic layers were washed with water and brine
  8. dry with materialdried over sodium sulfate
  9. customevaporated
  10. customto give a yellow oil

Sources & evidence

ORD record
ord-fd38f4450e1d494db79e8641c2906c25
Source dataset
uspto-grants-1998_12
Patent number
US05854249

Reaction notes

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