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[2-Bromo-4-(trifluoromethyl)benzyl]malonic acid → 3-(2-Bromo-4-(trifluoromethyl)phenyl)propanoic acid

HRID 1191910
Notes
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Reaction equation

HRID 1191910 reaction equation
[Br:1][C:2]1[CH:15]=[C:14]([C:16]([F:19])([F:18])[F:17])[CH:13]=[CH:12][C:3]=1[CH2:4][CH:5](C(O)=O)[C:6]([OH:8])=[O:7]>CCOCC>[Br:1][C:2]1[CH:15]=[C:14]([C:16]([F:19])([F:18])[F:17])[CH:13]=[CH:12][C:3]=1[CH2:4][CH2:5][C:6]([OH:8])=[O:7]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 22754130[2-Bromo-4-(trifluoromethyl)benzyl]malonic acid

Product 1

HCID 227541293-(2-Bromo-4-(trifluoromethyl)phenyl)propanoic acidYield 85%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

[2-Bromo-4-(trifluoromethyl)benzyl]malonic acid (9.80 g, 28.7 mmol) in a round-bottom flask was heated to 180° C. and heating was continued at 180° C. for 1.5 hrs. After cooling to room temperature, the solid was dissolved in ether. The resulting solution was dried over MgSO4 and concentrated. The solid was washed with hexane to give the title compound (7.20 g, 85%). MS calculated for C10H8BrF3O2: (M+H)+ 297. found 297.0, 299.0.

Workup

  • temperatureheating
  • dry with materialThe resulting solution was dried over MgSO4
  • concentrationconcentrated
  • washThe solid was washed with hexane
  • Sources & evidence

    ORD record
    ord-ba0a46cc6398414bb378d14f4f9c53ef
    Source dataset
    uspto-grants-2014_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08680104B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes