Reaktionsgleichung
[C:1]1([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([OH:14])[CH:9]=2)[CH:6]=[CH:5][CH:4]=[C:3]([OH:7])[CH:2]=1.Br[CH2:16][CH2:17][CH2:18][OH:19].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[OH:19][CH2:18][CH2:17][CH2:16][O:14][C:10]1[CH:9]=[C:8]([C:1]2[CH:6]=[CH:5][CH:4]=[C:3]([OH:7])[CH:2]=2)[CH:13]=[CH:12][CH:11]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
26.0 g (0.140 mol) of biphenyl-3,3′-diol and 10.0 g of 3-bromo-1-propanol are dissolved in 300 ml of acetone, and, after addition of 19.3 g (0.140 mol) of potassium carbonate, the mixture is heated under reflux overnight. The batch is subsequently filtered and evaporated, and the residue is chromatographed on silica gel with toluene/ethyl acetate (1:1), giving 3′-(3-hydroxypropoxy)biphenyl-3-ol as colourless crystals.
Aufarbeitung
- temperaturethe mixture is heated
- temperatureunder reflux overnight
- filtrationThe batch is subsequently filtered
- customevaporated
- customthe residue is chromatographed on silica gel with toluene/ethyl acetate (1:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-03f122dcbd154e85b85f04a9e58d140a
- Quelldatensatz
- uspto-grants-2012_11
- Patentnummer
- US08313669B2
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