Acetic Acid → HCID 19090879, compound

HRID 1463609Notes

Reaction equation

HRID 1463609 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

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-8e4a3e65ebf44fe686d885d3a4d4f1ae
Source dataset
uspto-grants-1994_04
Patent number
US05300679

Reaction notes

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