Reaktion #68748

ord-292f32fc9ab04384a8099dec217a1cbc

Reaktionsgleichung

CCc1ccc(-c2ccc(Cl)cc2)cc1Br
3-bromo-4′-chloro-4-ethylbiphenyl
[Mg]
magnesium
[Mg]
magnesium
II
iodine
O=Cc1ccco1
2-furaldehyde
CCc1ccc(-c2ccc(Cl)cc2)cc1Br
3-bromo-4′-chloro-4-ethylbiphenyl
CCc1ccc(-c2ccc(Cl)cc2)cc1C(O)c1ccco1
(4′-chloro-4-ethylbiphen-3-yl)furan-2-ylmethanol

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGstirred once
  2. 2
    Temperaturwarmed until the orange coloured mixture
  3. 3
    Temperaturwith external heating
  4. 4
    Temperaturto maintain a gentle reflux
  5. 5
    workup.ADDITIONOnce the addition
  6. 6
    Temperaturthe mixture is heated
  7. 7
    Temperaturcooled further in an ice-bath
  8. 8
    workup.STIRRINGthe mixture is stirred at room temperature overnight

Vorschrift

Approximately 10 ml of a solution of 3-bromo-4′-chloro-4-ethylbiphenyl (40.0 g, 135.3 mmol) in tetrahydrofuran (200 ml) is added to magnesium turnings in a dry flask, followed by a crystal of iodine. The mixture is allowed to stand without stirring for 30 minutes, then stirred once and warmed until the orange coloured mixture becomes colourless. The remainder of the 3-bromo-4′-chloro-4-ethylbiphenyl solution is added dropwise over 30 minutes with external heating applied as necessary to maintain a gentle reflux. Once the addition is complete, the mixture is heated to reflux for 2-3 hours, until only trace residues of magnesium remain. The mixture is cooled to room temperature, and then cooled further in an ice-bath. A solution of 2-furaldehyde (13.05 g, 135.8 mmol) in tetrahydrofuran (80 ml) is added dropwise over 35 minutes, and the mixture is stirred at room temperature overnight.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530388B2uspto-grants-2013_09