Methane → [Hydroxy(ethyl)phosphinyl]acetic acid

HRID 1028262Notes

Reaction equation

HRID 1028262 reaction equation
[CH2:1]([P:3]([CH2:6][CH2:7][OH:8])(=[O:5])[OH:4])[CH3:2].[OH-:9].[Na+].C.OO>O.[Pd]>[CH2:1]([P:3]([OH:4])([CH2:6][C:7]([OH:9])=[O:8])=[O:5])[CH3:2]

Participants

7

Conditions

Temperature
70 °C

Procedure

13.8 g (0.1 mol) of ethyl-(2-hydroxyethyl)phosphinic acid (produced as in Example 9) are dissolved in 150 ml of water and adjusted to pH 9 with 2N NaOH solution. Then, 0.25 g of charcoal with 5% Pd and 1% Bi is added, the suspension is heated to 70° C. and 30% strength hydrogen peroxide solution is passed into the suspension at a flow rate of 1 mol equivalent per hour. All the while, the pH of the suspension is maintained at pH=9 by adding 2N NaOH solution. After the reaction has ended, the reaction solution is filtered to remove the catalyst, which is washed, and the filtrate is made acidic with hydrochloric acid and the water is distilled off in vacuo. The residue is taken up in tetrahydrofuran and extracted. The insoluble salts are filtered off to leave 14.0 g (92% of theory) of 2-(ethylhydroxyphosphinyl)acetic acid as a colorless solid material.

Workup

  1. temperatureAll the while, the pH of the suspension is maintained at pH=9
  2. filtrationthe reaction solution is filtered
  3. customto remove the catalyst, which
  4. washis washed
  5. distillationthe water is distilled off in vacuo
  6. extractionextracted
  7. filtrationThe insoluble salts are filtered off

Sources & evidence

ORD record
ord-65bb3ec2a4dd4834b4bfb76f8b99a951
Source dataset
uspto-grants-2014_05
Patent number
US08735476B2

Reaction notes

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