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Diethyl (4-fluorophenyl)phosphonate → (4-Fluorophenyl)phosphonic acid

HRID 2041840
Notes
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Reaction equation

HRID 2041840 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([P:8](=[O:15])([O:12]CC)[O:9]CC)=[CH:4][CH:3]=1>Cl>[F:1][C:2]1[CH:3]=[CH:4][C:5]([P:8](=[O:9])([OH:15])[OH:12])=[CH:6][CH:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 13508438Diethyl (4-fluorophenyl)phosphonate

Product 1

HCID 12670622(4-Fluorophenyl)phosphonic acid

Reagents, catalysts & solvents 1

HCID 313Hydrochloric AcidSolvent

Procedure

Diethyl 4-fluorophenylphosphonate (600 mg, 2.55 mmol) was combined with 8M HCl (10 mL, excess) and the mixture refluxed overnight. The reaction was cooled and filtered to remove dark specks. The solvent was removed under vacuum until a solid began to form. The mixture was then put in the refrigerator for several hours. The solid was dried to yield an off-white powder (P80 mg). 1H NMR (400.14 MHz, DMSO) δ 7.71 (ddd, J=12.49, 8.52, 5.99 Hz, 2H), 7.28 (ddd, J=9.02, 9.02, 2.65 Hz, 2H). 31P{1H} NMR (161.97 MHz, DMSO): δ 12.81. Analysis calculated (found) %: C, 40.93 (40.33), H, 3.43 (3.49).

Workup

  1. temperaturethe mixture refluxed overnight
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • temperatureThe reaction was cooled
  • filtrationfiltered
  • customto remove dark specks
  • customThe solvent was removed under vacuum until a solid
  • customto form
  • waitThe mixture was then put in the refrigerator for several hours
  • customThe solid was dried
  • customto yield an off-white powder (P80 mg)
  • Sources & evidence

    ORD record
    ord-277c865f332b46abaee6991c20812382
    Source dataset
    uspto-grants-2013_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08586208B2

    Reaction notes

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