반응 #1995491

ord-376eb5933b6d42ce817511e2798b3e5d

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The resulting suspension is heated
  2. 2
    온도to reflux for 2 hours
  3. 3
    온도The reaction is cooled
  4. 4
    농축concentrated under reduced pressure
  5. 5
    여과the resulting solid is collected by filtration
  6. 6
    세척washed with H2O

실험 절차

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]+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08598210B2uspto-grants-2013_12