Reaktion #2275702
ord-645c1739639e405188ab22a011697c98
Reaktionsgleichung
4′-chloro-3-methoxy-biphenyl-4-carboxylic acid methyl ester
H2O
LiOH
→
desired product
Ausbeute 91.0%
4′-chloro-3-methoxy-biphenyl-4-carboxylic acid
Ausbeute 91.0%
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1TemperaturThe resulting suspension is heated
- 2Temperaturto reflux for 2 hours
- 3TemperaturThe reaction is cooled
- 4Einengenconcentrated under reduced pressure
- 5Filtrationthe resulting solid is collected by filtration
- 6Waschenwashed with H2O
- 7Sonstigedried
Vorschrift
To a solution of 4′-chloro-3-methoxy-biphenyl-4-carboxylic acid methyl ester, 8, (0.615 g, 2.22 mmol) in THF (20 mL) and H2O (5 mL) at room temperature is added LiOH (0.932 g, 22.2 mmol). The resulting suspension is heated to reflux for 2 hours. The reaction is cooled and concentrated under reduced pressure. The crude product is acidified using conc. HCl and the resulting solid is collected by filtration washed with H2O and dried to afford 0.532 g (91%) of the desired product as a grey solid. 1H NMR (400 MHz, CDCl3) δ ppm 10.69 (1H, br s), 8.26 (1H, d, J=8.1 Hz), 7.53-7.58 (2H, m), 7.44-7.50 (2H, m), 7.33 (1H, dd, J=8.1, 1.6 Hz), 7.20 (1H, d, J=1.3 Hz), 4.17 (3H, s). HPLC-MS: m/z 263 [M+H]+.