Réaction #2275702

ord-645c1739639e405188ab22a011697c98

Équation de réaction

COC(=O)c1ccc(-c2ccc(Cl)cc2)cc1OC
4′-chloro-3-methoxy-biphenyl-4-carboxylic acid methyl ester
O
H2O
[Li+].[OH-]
LiOH
COc1cc(-c2ccc(Cl)cc2)ccc1C(=O)O
desired product
Rendement 91.0%
COc1cc(-c2ccc(Cl)cc2)ccc1C(=O)O
4′-chloro-3-methoxy-biphenyl-4-carboxylic acid
Rendement 91.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe resulting suspension is heated
  2. 2
    Températureto reflux for 2 hours
  3. 3
    TempératureThe reaction is cooled
  4. 4
    Concentrationconcentrated under reduced pressure
  5. 5
    Filtrationthe resulting solid is collected by filtration
  6. 6
    Lavagewashed with H2O
  7. 7
    Autredried

Mode opératoire

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]+.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08323671B2uspto-grants-2012_12