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Formaldehyde → HCID 54405233, compound

HRID 866362
Notes
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Reaction equation

HRID 866362 reaction equation
[NH2:1][C:2]([P:8]([OH:11])(=[O:10])[OH:9])([P:4]([OH:7])(=[O:6])[OH:5])[CH3:3].C=O.P(Cl)(Cl)Cl>>[P:4]([CH:2]=[N:1][C:2]([P:4]([OH:7])(=[O:5])[OH:6])([P:8]([OH:11])(=[O:9])[OH:10])[CH3:3])([OH:7])([OH:6])=[O:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 712FormaldehydeHCID 24387Phosphorus trichlorideHCID 84770(1-Aminoethylidene)bisphosphonic acid

Product 1

HCID 54405233HCID 54405233, compound

Procedure

103 g. of 1-amino ethane-1,1-diphosphonic acid are suspended in 100 g. of a 30% formaldehyde solution. 85 cc. of phosphorus trichloride are added thereto drop by drop while stirring. After the addition is completed, the mixture is heated to boiling until a homogeneous mixture is formed. The water is removed by evaporation in a vacuum. The resulting phosphonic acid mixture is precipitated by the addition of acetone. N-phosphono methylene-1-amino ethane-1,1-diphosphonic acid is obtained in this manner.

Workup

  1. addition
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
After the addition
  • temperaturethe mixture is heated
  • customis formed
  • customThe water is removed by evaporation in a vacuum
  • customThe resulting phosphonic acid mixture is precipitated by the addition of acetone
  • Sources & evidence

    ORD record
    ord-1424e06f291248e488103bc1c490419e
    Source dataset
    uspto-grants-1978_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04098814

    Reaction notes

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