Diethylamine → 50362-13-5

HRID 1756807Notes

Reaction equation

HRID 1756807 reaction equation
[C:1]([OH:8])(=O)/[CH:2]=[CH:3]/[CH:4]=[CH:5]/[CH3:6].[CH2:9]([NH:11][CH2:12][CH3:13])[CH3:10].C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1>CN(C)C=O.C(OCC)(=O)C>[CH2:9]([N:11]([CH2:12][CH3:13])[C:1](=[O:8])/[CH:2]=[CH:3]/[CH:4]=[CH:5]/[CH3:6])[CH3:10]

Participants

6

Procedure

Sorbic acid (5.01 g, 44.7 mmol) and diethylamine (3.59 g, 49 mmol) were dissolved in dimethylformamide (100 ml) and the solution was stirred under ice-cooling. To the solution was added diphenylphosphoryl azide (15.0 g, 54.5 mmol) and the mixture was stirred for 20 hours while allowing to rise the temperature to room temperature. The reaction mixture was diluted with ethyl acetate and washed with an aqueous saturated sodium chloride solution. The ethyl acetate layer was washed with an aqueous saturated sodium carbonate and aqueous saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (chloroform:methanol=200:1-50:1) to obtain sorbic acid N,N-diethylamide (7.40 g, 99.9%) as pale yellow solid. This compound has the following NMR spectrum.

Workup

  1. temperaturecooling
  2. stirringthe mixture was stirred for 20 hours
  3. customto room temperature
  4. washwashed with an aqueous saturated sodium chloride solution
  5. washThe ethyl acetate layer was washed with an aqueous saturated sodium carbonate and aqueous saturated sodium chloride solution
  6. dry with materialdried over anhydrous sodium sulfate
  7. distillationThe solvent was distilled off under reduced pressure
  8. customthe residue was purified by silica gel column chromatography (chloroform:methanol=200:1-50:1)

Sources & evidence

ORD record
ord-cd03ccebf38d404cb6385c1036a9f915
Source dataset
uspto-grants-1995_08
Patent number
US05442062

Reaction notes

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