돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1835592생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1835592

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물4'-Benzyloxy-2'-hydroxyacetophenoneHCID 309257—
반응물6-Bromo-2,2-dimethylhexanenitrileHCID 4638215—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-(Benzyloxy)-2-[(5-methyl-5-cyanohexyl)oxy]-benzophenoneHCID 23501784111%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06770259B2
출처 데이터셋uspto-grants-2004_08
ORD IDord-d0a4102658d44d36b5d976d8d75ca7c9
출처 메모uspto-grants-2004_08