Acetic Acid → 1-[(4E,6E)-7-ethoxycarbonyl-1,1-dimethyl-4,6-heptadienyl]imidazole

HRID 127808Notes

Reaction equation

HRID 127808 reaction equation
[CH2:1]([O:3][C:4](/[CH:6]=[CH:7]/[CH2:8]P(=O)(OCC)OCC)=[O:5])[CH3:2].C([N-]C(C)C)(C)C.[Li+].[CH:25]([CH2:27][CH2:28][C:29]([N:32]1[CH:36]=[CH:35][N:34]=[CH:33]1)([CH3:31])[CH3:30])=O.C(O)(=O)C>O1CCCC1>[CH2:1]([O:3][C:4](/[CH:6]=[CH:7]/[CH:8]=[CH:25]/[CH2:27][CH2:28][C:29]([N:32]1[CH:36]=[CH:35][N:34]=[CH:33]1)([CH3:31])[CH3:30])=[O:5])[CH3:2]

Participants

6

Conditions

Temperature
-70 °C

Procedure

Under an atmosphere of nitrogen, 2.0 g of diethyl (E)-3-ethoxycarbonyl-2-propenylphosphonate was added dropwise to 25 ml of a 0.32 M solution of lithium diisopropylamide in tetrahydrofuran at -78° C. and the mixture was stirred at -70° C. for 30 minutes. To it was added a solution of 1.0 g of 1-(3-formyl-1,1-dimethylpropyl)imidazole (prepared as described hereafter) in 2 ml of tetrahydrofuran at -70° C., the mixture was stirred at room temperature for 30 minutes. To it was added 0.91 ml of acetic acid. After evaporation under reduced pressure, the residue was dissolved in chloroform, washed with a saturated aqueous solution of sodium bicarbonate, water, dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of chloroform and ethanol (99:1) as eluent to give 0.85 g of the title compound having the following physical characteristics:

Workup

  1. stirringthe mixture was stirred at room temperature for 30 minutes
  2. customAfter evaporation under reduced pressure
  3. dissolutionthe residue was dissolved in chloroform
  4. washwashed with a saturated aqueous solution of sodium bicarbonate, water
  5. dry with materialdried over sodium sulphate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by column chromatography on silica gel using
  8. additiona mixture of chloroform and ethanol (99:1) as eluent

Sources & evidence

ORD record
ord-2668a7fdf7194275a450519506545de5
Source dataset
uspto-grants-1981_03
Patent number
US04256757

Reaction notes

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