Benzyl Alcohol → 1-(4-Benzyloxy-3-trifluoromethyl-phenyl)-ethanone

HRID 2167836Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2167836
[CH2:1]([OH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CC([O-])(C)C.[K+].F[C:16]1[CH:21]=[CH:20][C:19]([C:22](=[O:24])[CH3:23])=[CH:18][C:17]=1[C:25]([F:28])([F:27])[F:26]>C1COCC1>[CH2:1]([O:8][C:16]1[CH:21]=[CH:20][C:19]([C:22](=[O:24])[CH3:23])=[CH:18][C:17]=1[C:25]([F:26])([F:27])[F:28])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

5

Edukt 3

HCID 244Benzyl AlcoholHCID 6056784'-Fluoro-3'-(trifluoromethyl)acetophenoneHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 670324791-(4-Benzyloxy-3-trifluoromethyl-phenyl)-ethanoneAusbeute 72,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A mixture of benzyl alcohol (10.9 mL; 104.98 mmol) and KOtBu (12.96 g; 115.5 mmol) in THF (500 mL) was heated under reflux for 10 minutes. Subsequently, 4′-fluoro-3′-(trifluoromethyl)acetophenone (21.64 g; 105 mmol) was added and the mixture heated under reflux for another 2 hours. After cooling to RT, the mixture was partitioned between EtOAc and a 5% aqueous NaHCO3 solution. The organic layer was separated, dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by column chromatography (SiO2, Et2O:hexanes 1:2.5) to afford 1-(4-Benzyloxy-3-trifluoromethyl-phenyl)-ethanone (22.37 g).

Aufarbeitung

  1. temperaturewas heated
  2. temperatureunder reflux for 10 minutes
  3. temperaturethe mixture heated
  4. temperatureunder reflux for another 2 hours
  5. customthe mixture was partitioned between EtOAc
  6. customThe organic layer was separated
  7. dry with materialdried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customThe residue was purified by column chromatography (SiO2, Et2O:hexanes 1:2.5)

Quellen und Nachweise

ORD-Eintrag
ord-7a375697b36a46c98e020a6e5c44723d
Quelldatensatz
uspto-grants-2015_06
Patentnummer
US09045441B2

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