2-Bromophenol → 1-Bromo-2-(2-ethylphenoxy)benzene

HRID 253554Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 253554
[CH2:1]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1B(O)O)[CH3:2].[Br:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[OH:19].CCN(CC)CC>C(Cl)Cl.CC([O-])=O.CC([O-])=O.[Cu+2]>[Br:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[O:19][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=1[CH2:1][CH3:2]

Komponenten

6

Versuchsvorschrift

To a solution of 2-ethylphenylboronic acid (4.50 g, 30 mmol), 2-bromophenol (3.54 g, 20 mmol), and Cu(OAc)2 (1.86 g, 10 mmol) in anhydrous CH2Cl2 (50 mL) were added activated 4 Å molecular sieves (˜0.5 g), followed by anhydrous Et3N (7.0 mL, 50 mmol). The resulting dark green solution was stirred at rt for 48 h. The solvent was removed under vacuum and the residue was triturated several times with ether (˜200 mL). The combined organic solutions were washed with satd aq NH4Cl, and 1 N aq HCl aqueous solution, and solvent was removed under vacuum to give a crude product. Flash column chromatography gave 1-bromo-2-(2-ethylphenoxy)benzene (1.72 g, 31%) as a clear oil; 1H NMR (CDCl3, 400 MHz) δ: 7.62 (dd, 1H), 7.28 (m, 1H), 7.22-7.08 (m, 3H), 6.96 (m, 1H), 6.78 (m, 2H), 2.64 (q, 2H), 1.22 (t, 3H); MS no ionization was observed.

Aufarbeitung

  1. customThe solvent was removed under vacuum
  2. customthe residue was triturated several times with ether (˜200 mL)
  3. washThe combined organic solutions were washed with satd aq NH4Cl, and 1 N aq HCl aqueous solution, and solvent
  4. customwas removed under vacuum
  5. customto give a crude product

Quellen und Nachweise

ORD-Eintrag
ord-43699f6428104e0ebb0068ca970a8f32
Quelldatensatz
uspto-grants-2011_01
Patentnummer
US07872028B2

Notizen zur Reaktion

Wird geladen…