Reaktion #73801

Reaktionsgleichung

4-Chlorophenylmagnesium bromide

4-bromobenzaldehyde

Water

→

title compound

(4-Bromo-phenyl)-(4-chloro-phenyl)-methanol

Lösungsmittel

tetrahydrofuran

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigethe solvent was removed under reduced pressure
2. 2
   SonstigeThe residue was then partitioned between ethyl acetate and 1N HCl solution
3. 3
   WaschenThe organic layer was washed with brine
4. 4
   Trocknendried (MgSO4)
5. 5
   Filtrationfiltered
6. 6
   Einengenconcentrated
7. 7
   SonstigeThe crude product was then purified by column chromatography (SiO2)
8. 8
   Wascheneluting with ethyl acetate/petroleum ether (1:9)

Vorschrift

4-Chlorophenylmagnesium bromide (12.97 ml, 1M solution in diethyl ether) was added slowly to a solution of 4-bromobenzaldehyde (2.0 g, 10.81 mmol) in tetrahydrofuran (25 ml) at 0° C., under an atmosphere of nitrogen. The reaction mixture was allowed to warm to room temperature and was stirred for 17 hours. Water (3 ml) was then added and the solvent was removed under reduced pressure. The residue was then partitioned between ethyl acetate and 1N HCl solution. The organic layer was washed with brine, dried (MgSO4), filtered and concentrated. The crude product was then purified by column chromatography (SiO2), eluting with ethyl acetate/petroleum ether (1:9), to yield the title compound (2.30 g). LC/MS: (PS-B3) Rt 3.49 [M−H]+ 297.

Quelle