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HRID 988940作成日:2026年10月25日

4-Methoxyphenol → 1-(3,7-Dimethyloctoxy)-4-methoxybenzene

https://huagongshe.com/reaction/988940

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethoxyphenolHCID 9015—
反応物Potassium HydroxideHCID 14797—
反応物1-Chloro-3,7-dimethyloctaneHCID 227360—
触媒Sodium IodideHCID 5238—
溶媒EthanolHCID 702—
生成物1-(3,7-Dimethyloctoxy)-4-methoxybenzeneHCID 515359195.3%

反応手順

184.4 g (1.48 mol) of p-methoxyphenol, 275.9 g (1.56 mol, 1.05 eq) of 3,7-dimethyl-1-octyl chloride, 106.9 g of KOH (85% strength, 1.62 mol, 1.09 eq) and 15.04 g of sodium iodide were dissolved in 620 ml of dry ethanol in a 2 l four-necked round-bottomed flask fitted with dropping funnel, high-efficiency condenser, gas outlet and magnetic stirrer bar, and heated at the boil for 64 hours with magnetic stirring. The mixture was cooled to room temperature, and the reaction solution was decanted off from the solid formed. The reaction solution was evaporated in a rotary evaporator. The solid was taken up in 400 ml of 10% strength aqueous NaOH solution. This solution was extracted twice with 400 ml of toluene each time. The organic phases were combined, washed with 100 ml of 10% strength aqueous NaOH solution and dried using Na2SO4. The solvent was distilled off under reduced pressure in a rotary evaporator. The residue was distilled under reduced pressure (1 mbar, head temperature: 159-162° C.), giving 372.4 g (1.41 mol, 95%) of 1-methoxy-4-(3,7-dimethyloctyloxy)benzene as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06638646B2
出典データセットuspto-grants-2003_10
ORD IDord-bd1e80158c0b4995ab7ce813b3cc2e91
出典メモuspto-grants-2003_10