反応 #70201

反応方程式

ketone

2′-Iodo-5′-isopropoxy-4′-methoxyacetophenone

AlCl3

→

title compound 13

収率 75.3%

5′-Hydroxy-2′-iodo-4′-methoxyacetophenone

収率 75.3%

溶媒

CH2Cl2

反応条件

後処理

1. 1
   その他then partitioned between H2O (10 mL) and additional CH2Cl2 (10 mL)
2. 2
   抽出The separated aqueous phase was extracted with CH2Cl2 (1×10 mL)
3. 3
   乾燥the combined organic fractions were then dried (MgSO4)
4. 4
   ろ過filtered
5. 5
   濃縮concentrated under reduced pressure
6. 6
   洗浄The ensuing residue was subjected to flash chromatography (1:4 v/v ethyl acetate/hexane elution)

実験手順

A solution of ketone 9 (625 mg, 1.87 mmol) in dry CH2Cl2 (5 mL), was treated with AlCl3 (325 mg, 2.44 mmol) and the resulting mixture stirred at 18° C. under a nitrogen atmosphere for 21 h then partitioned between H2O (10 mL) and additional CH2Cl2 (10 mL). The separated aqueous phase was extracted with CH2Cl2 (1×10 mL) and the combined organic fractions were then dried (MgSO4), filtered and concentrated under reduced pressure. The ensuing residue was subjected to flash chromatography (1:4 v/v ethyl acetate/hexane elution) to afford the title compound 13 (411 mg, 75%) as a pale-yellow solid, m.p. 109.4-110.6° C., Rf 0.5 in 1:1 v/v ethyl acetate/hexane.

出典