Reaktion #70220

Reaktionsgleichung

ketone

2′-Bromo-5′-isopropoxy-4′-methoxyacetophenone

AlCl3

→

title compound 39

Ausbeute 98.0%

2′-Bromo-5′-hydroxy-4′-methoxyacetophenone

Ausbeute 98.0%

Lösungsmittel

CH2Cl2

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe ensuing mixture was partitioned between H2O (5 mL) and CH2Cl2 (5 mL)
2. 2
   Extraktionthe separated aqueous phase extracted with CH2Cl2 (1×15 mL)
3. 3
   TrocknenThe combined organic fractions were dried (MgSO4)
4. 4
   Filtrationfiltered
5. 5
   Einengenconcentrated under reduced pressure
6. 6
   Waschenthe ensuing residue subjected to flash chromatography (15:85 v/v ethyl acetate/hexane elution)

Vorschrift

A solution of ketone 38 (220 mg, 0.766 mmol) in dry CH2Cl2 (2.0 mL) was treated with AlCl3 (306 mg, 2.29 mmol) and the resulting mixture stirred at 18° C. under a nitrogen atmosphere for 2 h. The ensuing mixture was partitioned between H2O (5 mL) and CH2Cl2 (5 mL) then the separated aqueous phase extracted with CH2Cl2 (1×15 mL). The combined organic fractions were dried (MgSO4), filtered and concentrated under reduced pressure and the ensuing residue subjected to flash chromatography (15:85 v/v ethyl acetate/hexane elution) to afford the title compound 39 (184 mg, 98%) as a pale-yellow solid, m.p. 109.7-111.4° C., Rf 0.4 in 1:1 v/v ethyl acetate/hexane.

Quelle