Hydrochloric Acid → 2-Methoxy-3'-carboethoxy-[1,1'-biphenyl]-6-carboxylic acid, ethyl ester

HRID 275172ノート

反応式

HRID 275172 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]([OH:11])=[O:10])[C:4]=1[C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([O:20][CH2:21][CH3:22])=[O:19])[CH:13]=1.Cl.[CH3:24][CH2:25]OC(C)=O.CCCCCC>CCO>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]([O:11][CH2:24][CH3:25])=[O:10])[C:4]=1[C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([O:20][CH2:21][CH3:22])=[O:19])[CH:13]=1

参加物

5

実験手順

Acid 5a (0.583 g., 1.90 mmol, 1 equiv.) is dissolved in 12 mL of absolute EtOH. Concentrated HCl (0.6 mL) is added, and the mixture heated to reflux for 24 hours. The mixture is then partitioned between EtOAc and water. The organic phase is washed with brine, dried (MgSO4), and concentrated in vacuo. Chromatography on silica gel using 5%, then 10% EtOAc/hexane yields 2-methoxy-3'-carboethoxy-[1,1'-biphenyl]-6-carboxylic acid, ethyl ester (6a) (0.432 g., 1.32 mmol, 73%) as a clear oil: UVmax (CHCl3) 242 nm (ε=12036), 296 nm (ε=4724); 1H NMR (300 MHz, CDCl3) δ 8.01 (m, 1H, ArH), 7.92 (m, 1H, ArH), 7.47-7.40 (m, 3H, ArH), 7.39 (dd, J=8, 8 Hz, 1H, ArH), 7.09 (dd, J= 2, 8 Hz, 1H, ArH), 4.34 (q, J=7 Hz, 2H, CO2CH2), 3.98 (q, J=7 Hz, 2H, CO2CH2), 3.73 (s, 3H, OCH3), 1.35 (t, J=7 Hz, 3H, CH2CH3), 0.91 (t, J=7 Hz, 3H, CH2CH3); 13C NMR (75 MHz, CDCl3) δ 168.04 (C=O), 166.65 (C=O), 156.92, 137.28, 134.11, 133.22, 130.73, 130.07, 129.98, 128.78, 128.22, 127.63, 121.63, 113.87, 60.88, 56.02, 14.34, 13.65; IR (film) 2982, 1718, 1466, 1366, 1298, 1260, 1234, 1110, 1060 cm-1 ; MS (DCI) m/e 329 (MH+), 283 (M--C2H5O). Anal. Calcd for C19H20O5 : C, 69.50; H, 6.14. Found: C, 69.44; H, 6.19.

後処理

  1. temperaturethe mixture heated
  2. temperatureto reflux for 24 hours
  3. customThe mixture is then partitioned between EtOAc and water
  4. washThe organic phase is washed with brine
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-6443cfb4ba7241ae96d486ebe5db8617
出典データセット
uspto-grants-1995_02
特許番号
US05391817

反応ノート

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