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HRID 1835592作成日:2026年10月26日

Potassium Iodide → 4-(Benzyloxy)-2-[(5-methyl-5-cyanohexyl)oxy]-benzophenone

https://huagongshe.com/reaction/1835592

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物4'-Benzyloxy-2'-hydroxyacetophenoneHCID 309257—
反応物6-Bromo-2,2-dimethylhexanenitrileHCID 4638215—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-(Benzyloxy)-2-[(5-methyl-5-cyanohexyl)oxy]-benzophenoneHCID 23501784111%

反応手順

A solution of 4-benzyloxy-2-hydroxyacetophenone (2.45 g), potassium carbonate (3.25 g), potassium iodide (0.42 g), and 5-cyano-5-methyl-1-bromohexane (2.6 g) in dimethylformamide (40 mL) was heated at 90° C. for 22 hours under nitrogen. The slurry was cooled, poured into water (150 mL) and extracted with ethyl acetate. The combined extracts were washed with water, dried (MgSO4), filtered, and concentrated under reduced pressure to an orange oil. This was purified by flash chromatography (ethyl acetate:hexane) to afford the product (2.4 g) as a clear oil. NMR(CDCl3): 1.37, s (6H); 1.64, m (4H); 1.89, m (2H); 2.58, s (3H); 4.03, t (3H); 5.09, s (2H); 6.50, s (1H); 6.58, d (1H); 7.37, m (5 H); 7.81, d (1H). Mass Spec (GC-MS) m/z=365 (M).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06770259B2
出典データセットuspto-grants-2004_08
ORD IDord-d0a4102658d44d36b5d976d8d75ca7c9
出典メモuspto-grants-2004_08