Acetone → HCID 86744760, compound

HRID 973628Notes

Reaction equation

HRID 973628 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][P:5]([OH:7])[OH:6].[CH3:8][C:9]([CH3:11])=[O:10].C(O)C.[ClH:15]>C[Si](C)(C)N[Si](C)(C)C.O>[ClH:15].[NH2:1][CH2:2][CH2:3][CH2:4][P:5]([C:9]([OH:10])([CH3:11])[CH3:8])(=[O:7])[OH:6]

Participants

7

Procedure

A suspension of 1.23 g 3-aminopropylphosphonous acid in 25 ml of hexamethyldisilazane is heated to reflux under an inert gas for 20 hours. After this time a clear solution results and the reaction mixture is cooled to room temperature under inert gas and 50 ml of anhydrous acetone is added and an exothermic reaction results. The reaction mixture is allowed to cool to room temperature and the volatile components removed in vacuo to afford a clear oil. This oil is dissolved in 50 ml of a 2.0M hydrochloric acid solution in water and washed with 2×100 ml of dichloromethane and 1×100 ml of ether. The aqueous layer is evaporated to dryness to give a semi-solid residue which is co-evaporated with water (10×20 ml) and absolute ethanol (10×20 ml yielding 3-aminopropyl(2-hydroxyprop-2-y)phosphinic acid hydrochloride m.p. 159°-161° as a white solid. This is suspended in absolute ethanol and treated with propylene oxide. Filtration and drying of the solid affords 3-aminopropyl(2-hydroxyprop-2 -yl)phosphinic acid; m.p. 243°-244°.

Workup

  1. temperatureis heated
  2. temperatureto reflux under an inert gas for 20 hours
  3. customAfter this time a clear solution results
  4. additionis added
  5. customan exothermic reaction
  6. customresults
  7. customthe volatile components removed in vacuo
  8. customto afford a clear oil
  9. washwashed with 2×100 ml of dichloromethane and 1×100 ml of ether
  10. customThe aqueous layer is evaporated to dryness
  11. customto give a semi-solid residue which

Sources & evidence

ORD record
ord-8d00761417254e90a17e3c28d3920dea
Source dataset
uspto-grants-1991_11
Patent number
US05064819

Reaction notes

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