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HRID 1704071作成日:2026年10月26日

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

https://huagongshe.com/reaction/1704071

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Sodium MethoxideHCID 10942334—
反応物4-Chloro-5,6,7,8-tetrahydronaphthalen-1-olHCID 20203333—
反応物Methyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 20392594—
溶媒BenzeneHCID 241—
溶媒WaterHCID 962—
生成物Methyl alpha-(4-chloro-5,6,7,8-tetrahydro-1-naphthyloxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetateHCID 12531871—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04125729
出典データセットuspto-grants-1978_11
ORD IDord-a7dea91b10574a23b43ba5fcb56dcb90
出典メモuspto-grants-1978_11