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HCID 19014057, compound → HCID 19014054, compound

HRID 1728538
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Reaction equation

HRID 1728538 reaction equation
C([CH:5]([C:17]([OH:19])=[O:18])[O:6][C:7]1[CH:8]=[C:9]([CH2:13][C:14](=[O:16])[CH3:15])[CH:10]=[CH:11][CH:12]=1)(C)(C)C>FC(F)(F)C(O)=O>[C:17]([CH2:5][O:6][C:7]1[CH:8]=[C:9]([CH2:13][C:14](=[O:16])[CH3:15])[CH:10]=[CH:11][CH:12]=1)([OH:19])=[O:18]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 19014057HCID 19014057, compound

Product 1

HCID 19014054HCID 19014054, compound

Reagents, catalysts & solvents 1

HCID 6422Trifluoroacetic acidSolvent

Procedure

To m-(t-butylcarboxymethoxy)phenyl acetone, 6.7 g, was added trifluoroacetic acid (40 ml) at room temperature under nitrogen. After five minutes, reaction was found to be completed by tlc (silica gel eluted with 1:9 parts by volume methanol:methylene chloride) and the solvent was then evaporated to dryness. The resulting brown oil showed the desired product and trace of starting material on tlc. IR showed characteristic carboxylic acid peak at 3600-2450 cm-1.

Workup

  1. customreaction
  2. washto be completed by tlc (silica gel eluted with 1:9 parts by volume methanol:methylene chloride)
  • customthe solvent was then evaporated to dryness
  • Sources & evidence

    ORD record
    ord-34af3a6a82bf4e8985c14aaaf35e4e9d
    Source dataset
    uspto-grants-1994_07
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05328828

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes