Acetic Acid → HCID 10330332, compound

HRID 1198821Notes

Reaction equation

HRID 1198821 reaction equation
[Na].[F:2][CH:3]([F:9])[PH:4](=[O:8])[O:5][CH2:6][CH3:7].[C:10](#[N:12])[CH3:11].[C:13](O)(=O)C>C(O)C>[C:10]([CH2:11][CH2:13][P:4]([CH:3]([F:9])[F:2])(=[O:8])[O:5][CH2:6][CH3:7])#[N:12]

Participants

6

Procedure

660 mg (28.8 mmol) of sodium are dissolved in 40 ml of ethanol. The solution is cooled to -10° and 8.6 g (57.6 mmol) of ethyl P-difluoromethylphosphinate and 3.8 ml (57.6 mmol) of acetonitrile are added with stirring. The reaction mixture is then allowed to warm up to room temperature and stirred for additional 17 hours and then adjusted to pH 6 by addition of glacial acetic acid. The solvents are evaporated and the residue is dissolved in dichloromethane, washed twice with water, dried over magnesium sulphate and evaporated to dryness. The crude product is purified by chromatography on silica gel with ethyl acetate/dichloromethane (7:3) as eluent. The fractions containing the desired product are combined and evaporated to dryness yielding ethyl P-(2-cyanoethyl)-P-difluoromethyl-phosphinate as an oil of Rf =0.54 (above eluent).

Workup

  1. temperatureThe solution is cooled to -10°
  2. stirringstirred for additional 17 hours
  3. customThe solvents are evaporated
  4. dissolutionthe residue is dissolved in dichloromethane
  5. washwashed twice with water
  6. dry with materialdried over magnesium sulphate
  7. customevaporated to dryness
  8. customThe crude product is purified by chromatography on silica gel with ethyl acetate/dichloromethane (7:3) as eluent
  9. additionThe fractions containing the desired product
  10. customevaporated to dryness

Sources & evidence

ORD record
ord-2563a3db21ad4b24b6613369bfd86ebc
Source dataset
uspto-grants-1994_01
Patent number
US05281747

Reaction notes

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