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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1863333생성일: 2026년 10월 25일

Potassium Iodide → Methyl alpha-(4-chloro-5,6,7,8-tetrahydro-1-naphthyloxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate

https://huagongshe.com/reaction/1863333

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium MethoxideHCID 10942334—
반응물4-Chloro-5,6,7,8-tetrahydronaphthalen-1-olHCID 20203333—
반응물Methyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
용매BenzeneHCID 241—
용매WaterHCID 962—
생성물Methyl alpha-(4-chloro-5,6,7,8-tetrahydro-1-naphthyloxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 12531871—

반응 단계

To a solution of 1.19 g of sodium methoxide, 4.57 g of 4-chloro-5,6,7,8-tetrahydro-1-naphthol, and 100 mg of potassium iodide was added 7.11 g of methyl α-bromo-α-[p-(p-chlorophenoxy)phenyl]acetate in 10 ml of benzene. The mixture was heated at reflux overnight, cooled to room temperature, and poured into 100 ml of water. The mixture was then extracted with 2×75 ml of ether. The combined extracts were washed with 2×50 ml of 5% NaOH, 2×50 ml of water, 50 ml of saturated brine, and dried (MgSO4). Evaporation of the solvent yielded an oil which was chromatographed over 100 g of silica gel (benzene). Concentration of cuts yielded a yellow gum which solidified on standing to give the product as a white solid, mp 87.5°-90° C. (6.4 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04168385
출처 데이터셋uspto-grants-1979_09
ORD IDord-740e6d6ca3204dcc9b4ca04665a9ca90
출처 메모uspto-grants-1979_09