Acetic Acid → HCID 19090879, compound

HRID 2050709Notes

Reaction equation

HRID 2050709 reaction equation
[O-]CC.[Na+].[C:5](#[N:8])[CH:6]=[CH2:7].[CH2:9]([O:12][P:13]([CH:15]([O:20][CH2:21][CH2:22][CH3:23])[O:16][CH2:17][CH2:18][CH3:19])[OH:14])[CH2:10]C.C(O)(=O)C>C(O)C>[C:5]([CH2:6][CH2:7][P:13]([CH:15]([O:16][CH2:17][CH2:18][CH3:19])[O:20][CH2:21][CH2:22][CH3:23])(=[O:14])[O:12][CH2:9][CH3:10])#[N:8]

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 7855AcrylonitrileHCID 2723922Sodium ethoxideHCID 53942597HCID 53942597, compound

Product 1

HCID 19090879HCID 19090879, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent2×

Procedure

A solution of sodium ethoxide in absolute ethanol (0.48 g of sodium metal in 15 ml of absolute ethanol) is cooled to 0° under nitrogen or argon. A solution of 2.72 g of acrylonitrile and 12.2 g of di-n-propyloxymethylphosphonous acid n-propylester in 50 ml of absolute ethanol is added at such a rate that the temperature does not exceed 5°. After the addition is completed, the solution is allowed to warm to room temperature and stirred overnight. After addition of 1.22 g of glacial acetic acid, the reaction mixture is concentrated in vacuo. The residue is partitioned between ethyl acetate and water and the organic phase separated. After drying over anhydrous magnesium sulphate the solvent is evaporated in vacuo to afford an oil. Chromatography on silica-gel yields ethyl 2-cyanoethyl(di-n-propyloxymethyl)phosphinate as a colourless oil.

Workup

  1. customdoes not exceed 5°
  2. additionAfter the addition
  3. concentrationthe reaction mixture is concentrated in vacuo
  4. customThe residue is partitioned between ethyl acetate and water
  5. customthe organic phase separated
  6. dry with materialAfter drying over anhydrous magnesium sulphate the solvent
  7. customis evaporated in vacuo
  8. customto afford an oil

Sources & evidence

ORD record
ord-7a70b60f68944f0fb9f7b997dd5b7d46
Source dataset
uspto-grants-1991_05
Patent number
US05013863

Reaction notes

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