反応 #2275719

ord-b65dd98d09304d329a6bee4db114f73d

反応方程式

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 compound
収率 91.0%
COc1cc(-c2ccc(Cl)cc2)ccc1C(=O)O
4′-chloro-3-methoxy-biphenyl-4-carboxylic acid
収率 91.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The resulting suspension is heated
  2. 2
    温度to reflux for 2 hours
  3. 3
    温度The reaction is cooled
  4. 4
    濃縮concentrated under reduced pressure
  5. 5
    ろ過the resulting solid is collected by filtration
  6. 6
    洗浄washed with H2O

実験手順

To a solution of 4′-chloro-3-methoxy-biphenyl-4-carboxylic acid methyl ester, 30, (0.615 g, 2.22 mmol) in THF (20 mL) and H2O (5 mL) 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 to afford 0.532 g (91% yield) of the desired compound 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]+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08323671B2uspto-grants-2012_12