Methane → [Hydroxy(ethyl)phosphinyl]acetic acid

HRID 1526928Notes

Reaction equation

HRID 1526928 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 (prepared as in Example 8) 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, 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-(ethylhydroxy-phosphinyl)acetic acid as colorless solid.

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-c0b163846b40451d866ba7848ec3ef35
Source dataset
uspto-grants-2015_07
Patent number
US09085734B2

Reaction notes

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