1,4-Dibromobenzene → 1-(4-Bromophenyl)cyclobutanol

HRID 19764

Reaktionsgleichung

Reaktionsgleichung von HRID 19764
Br[C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[CH:4][CH:3]=1.[Li]CCCC.[C:14]1(=[O:18])[CH2:17][CH2:16][CH2:15]1.[NH4+].[Cl-]>CCOCC.O>[Br:8][C:5]1[CH:6]=[CH:7][C:2]([C:14]2([OH:18])[CH2:17][CH2:16][CH2:15]2)=[CH:3][CH:4]=1

Komponenten

7

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a solution of 1,4-dibromobenzene (1.00 g, 4.24 mmol) at −78° C. in ether (20 ml) was added n-BuLi (2.65 ml, 1.6 M solution in hexane, 4.24 mmol) and the reaction mixture was stirred at −78° C. for 30 min. Cyclobutanone (348 μl, 4.66 mmol) was then added and the reaction mixture was stirred at −78° C. for 15 min. The reaction mixture was then slowly (over 2 h) warmed to 0° C. and stirred for a further 1 h. Water was added followed by sat. NH4Cl and the reaction mixture was extracted with ether. The organic layer was washed with brine, dried (MgSO4), filtered and concentrated in vacuo to give a residue which was purified by flash column chromatography (1:4 ether/pentane) to give 1-(4-bromophenyl)-cyclobutanol (330 mg, 34%) as a colorless oil. 1H NMR (CDCl3, 300 MHz): δ 7.50 (d, J=8.5 Hz, 2H), 7.38 (d, J=8.5 Hz, 2H), 2.57-2.48 (m, 2H), 2.41-2.31 (m, 2H), 2.02 (m, 1H), 1.69 (m, 1H).

Aufarbeitung

  1. stirringthe reaction mixture was stirred at −78° C. for 15 min
  2. temperatureslowly (over 2 h) warmed to 0° C.
  3. stirringstirred for a further 1 h
  4. extractionthe reaction mixture was extracted with ether
  5. washThe organic layer was washed with brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customto give a residue which
  10. customwas purified by flash column chromatography (1:4 ether/pentane)

Quellen und Nachweise

ORD-Eintrag
ord-d76891fc0c314df8919a1a6861f1cf2a
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07745477B2

Verknüpfte Notizen

Wird geladen…