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Tert-butyl 4-(2,4-difluorophenyl)-2-(4-fluorobenzamido)benzoate → 4-(2,4-Difluorophenyl)-2-(4-fluorobenzamido)benzoic acid

HRID 1673430
Notes
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Reaction equation

HRID 1673430 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[CH:21]=[CH:20][C:12]([C:13]([O:15]C(C)(C)C)=[O:14])=[C:11]([NH:22][C:23](=[O:31])[C:24]2[CH:29]=[CH:28][C:27]([F:30])=[CH:26][CH:25]=2)[CH:10]=1>FC(F)(F)C(O)=O>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9]1[CH:21]=[CH:20][C:12]([C:13]([OH:15])=[O:14])=[C:11]([NH:22][C:23](=[O:31])[C:24]2[CH:29]=[CH:28][C:27]([F:30])=[CH:26][CH:25]=2)[CH:10]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 67342274Tert-butyl 4-(2,4-difluorophenyl)-2-(4-fluorobenzamido)benzoate

Product 1

HCID 673429254-(2,4-Difluorophenyl)-2-(4-fluorobenzamido)benzoic acid

Reagents, catalysts & solvents 1

HCID 6422Trifluoroacetic acidSolvent

Procedure

10 mL of trifluoroacetic acid was added to the obtained tert-butyl 4-(2,4-difluorophenyl)-2-(4-fluorobenzamido)benzoate and stirred at room temperature for 2 hours. The solvent was evaporated under reduced pressure and diisopropyl ether was added to the obtained residue and a solid substance was separated by filtration to obtain 46 mg of 4-(2,4-difluorophenyl)-2-(4-fluorobenzamido)benzoic acid as white solid.

Workup

  • customThe solvent was evaporated under reduced pressure and diisopropyl ether
  • additionwas added to the obtained residue
  • customa solid substance was separated by filtration
  • Sources & evidence

    ORD record
    ord-1a7592d84d074252a32db9c47532f740
    Source dataset
    uspto-grants-2011_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07999132B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes