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

HRID 1740592
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1740592
[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]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 27772232-(Trifluoromethoxy)benzoic acid

Produkt 1

HCID 27772452-(Trifluoromethoxy)benzyl alcohol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

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)).

Aufarbeitung

  • customThe 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
  • Quellen und Nachweise

    ORD-Eintrag
    ord-cc76186cf83940e79fb194eed7bb111c
    Quelldatensatz
    uspto-grants-1999_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US05968938

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