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2-(Trifluoromethoxy)benzoic acid → 2-(Trifluoromethoxy)benzyl alcohol

HRID 1740592
Notes
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Reaction equation

HRID 1740592 reaction equation
[F:1][C:2]([F:14])([F:13])[O:3][C:4]1[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=1[C:6](O)=[O:7]>C1COCC1>[F:1][C:2]([F:13])([F:14])[O:3][C:4]1[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=1[CH2:6][OH:7]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 27772232-(Trifluoromethoxy)benzoic acid

Product 1

HCID 27772452-(Trifluoromethoxy)benzyl alcohol

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

To a stirred solution of 2-trifluoromethoxybenzoic acid (1.0 g, 5.2 mmol) in THF (25 mL) at 0° C. was added borane-THF complex (15 mL of a 1.0 M solution in THF, 15 mmol). The solution was warmed to ambient temperature and stirred for 14 h. The solvent was removed under reduced pressure and the residue was partitioned between EtOAc (75 mL) and saturated aqueous NaHCO3 (75 mL). The organic phase was dried (MgSO4), filtered and the solvent was removed under reduced pressure to give 2-trifluoromethoxybenzyl alcohol as a colorless liquid (TLC Rf =0.2 (1:3 EtOAc-hexanes)).

Workup

custom
The solvent was removed under reduced pressure
  • customthe residue was partitioned between EtOAc (75 mL) and saturated aqueous NaHCO3 (75 mL)
  • dry with materialThe organic phase was dried (MgSO4)
  • filtrationfiltered
  • customthe solvent was removed under reduced pressure
  • Sources & evidence

    ORD record
    ord-cc76186cf83940e79fb194eed7bb111c
    Source dataset
    uspto-grants-1999_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05968938

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes