Water → 2-Benzyloxy-5-(trifluoromethoxy)benzene

HRID 617722Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 617722
[CH2:1](Br)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:9][C:10]([F:20])([F:19])[O:11][C:12]1[CH:17]=[CH:16][C:15]([OH:18])=[CH:14][CH:13]=1.C(=O)([O-])[O-].[K+].[K+].O>CN(C)C=O>[CH2:1]([O:18][C:15]1[CH:16]=[CH:17][C:12]([O:11][C:10]([F:9])([F:19])[F:20])=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

6

Edukt 4

HCID 962WaterHCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 70015p-(Trifluoromethoxy)phenol

Produkt 1

HCID 215840942-Benzyloxy-5-(trifluoromethoxy)benzeneAusbeute 99 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

Benzyl bromide (66.17 ml, 95.35 g, 0.56mol) was added to a mixture of 4-(trifluoromethoxy)phenol (90.26 g, 0.51mol) and potassium carbonate (140.97 g, 1.2mol) in dimethylformamide (160 ml) and the mixture was stirred at room temperature for 72 hours. The mixture was poured into water (1.5 l) and extracted with ethyl acetate (3×500 ml). The combined organic fractions were washed with aqueous sodium carbonate (saturated, 500 ml), dried (MgSO4) and the solvent was evaporated under reduced pressure to give the title compound as a colorless solid (133.5 g, 99%). 1H NMR (360 MHz, CDCl3) δ 7.39 (5H, m), 7.14 (2H, d, J=9.0 Hz), 6.95 (2H, d, J=9.0 Hz), and 5.05 (2H, s).

Aufarbeitung

  1. extractionextracted with ethyl acetate (3×500 ml)
  2. washThe combined organic fractions were washed with aqueous sodium carbonate (saturated, 500 ml)
  3. dry with materialdried (MgSO4)
  4. customthe solvent was evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-9e6d89563290408ba29dcac8d21b17a0
Quelldatensatz
uspto-grants-1999_09
Patentnummer
US05952315

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