Acetic Acid → 3-Methoxy-3'-(6-(trifluoromethyl)pyridin-2-yl)biphenyl-4-ol

HRID 42640Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 42640
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([C:27]([F:30])([F:29])[F:28])[N:22]=3)[CH:16]=2)=[CH:11][C:10]=1[O:31][CH3:32])C1C=CC=CC=1.Br.C(O)(=O)C>ClCCl>[CH3:32][O:31][C:10]1[CH:11]=[C:12]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([C:21]3[CH:26]=[CH:25][CH:24]=[C:23]([C:27]([F:30])([F:28])[F:29])[N:22]=3)[CH:16]=2)[CH:13]=[CH:14][C:9]=1[OH:8]

Komponenten

5

Versuchsvorschrift

To a solution of 2-(4′-(benzyloxy)-3′-methoxybiphenyl-3-yl)-6-(trifluoromethyl)pyridine (1.061 g, 2.44 mmol) in dichloromethane (20 mL) cooled in an ice-water bath was added a 30% solution of hydrogen bromide in acetic acid (4 mL, 20 mmol) dropwise. The resulting solution was allowed to stir at room temperature for six hours then poured onto ice-water (100 mL). The phases were separated and the aqueous phase was extracted with dichloromethane (10 mL). The combined organic layers were washed with water and brine, then dried over anhydrous sodium sulphate and filtered. Evaporation of the solvent left a brown oil that was chromatographed over silica gel (petroleum ether/ethyl acetate, 4:1) to give 3-methoxy-3′-(6-(trifluoromethyl)pyridin-2-yl)biphenyl-4-ol as a clear oil, 0.547 g (65%).

Aufarbeitung

  1. additionthen poured onto ice-water (100 mL)
  2. customThe phases were separated
  3. extractionthe aqueous phase was extracted with dichloromethane (10 mL)
  4. washThe combined organic layers were washed with water and brine
  5. dry with materialdried over anhydrous sodium sulphate
  6. filtrationfiltered
  7. customEvaporation of the solvent
  8. waitleft a brown oil that
  9. customwas chromatographed over silica gel (petroleum ether/ethyl acetate, 4:1)

Quellen und Nachweise

ORD-Eintrag
ord-983ebd0c0ebc4d28820d26ad5f153b3f
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08536203B2

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