Hydrochloric Acid → 4-Biphenylylacetic acid methyl ester
Reaktionsgleichung
[C:1]1([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:6]=[CH:5][C:4]([CH2:7][C:8]([OH:10])=[O:9])=[CH:3][CH:2]=1.Cl.[CH3:18]O>>[CH3:18][O:9][C:8](=[O:10])[CH2:7][C:4]1[CH:3]=[CH:2][C:1]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)=[CH:6][CH:5]=1Komponenten
4
Versuchsvorschrift
To a solution of 4-biphenylacetic acid (10 g, 47 mmol) in methanol (150 mL) was added concentrated HCl (3 mL). The mixture was heated under reflux for 16 hours, cooled to rt, and the solvent was evaporated. Chromatography of the residue over silica gel (petroleum ether followed by ethyl acetate/petroleum ether 1/4) gave 4-biphenylacetic acid methyl ester (10.4 g, 98%).
Aufarbeitung
- temperatureThe mixture was heated
- temperatureunder reflux for 16 hours
- customthe solvent was evaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-222d54d649a9420e8a0f0f3797bde1cf
- Quelldatensatz
- uspto-grants-2000_04
- Patentnummer
- US06054470
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