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HRID 347395作成日:2026年10月26日

1,4-Dimethoxybenzene → 1-Acetoxy-2-methyl-3-(2,5-dimethoxyphenyl)propene

https://huagongshe.com/reaction/347395

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DimethoxybenzeneHCID 9016—
反応物Methacrolein diacetateHCID 25305—
溶媒Ethyl AcetateHCID 8857—
生成物1-Acetoxy-2-methyl-3-(2,5-dimethoxyphenyl)propeneHCID 6946538677.4%

反応条件

温度53.5 °C

反応手順

In an argon gas atmosphere, a three necked flask having a capacity of 25 ml was charged with 1.92 g (10 m moles) of 3,3-diacetoxy-2-methylpropene having a purity degree of 89.6% by mass and 13.82 g (100 m moles) of hydroquinone dimethylether. Then, the resultant mixture was mixed with 0.14 g (1 m mole) of boron trifluoride-diethyl ether complex at an internal temperature of 54° C. over a time of one minute. The mixture was stirred at an internal temperature of 53 to 54° C. for one hour to cause the mixed compounds to react with each other. After the reaction was completed, the resultant reaction liquid was mixed with 150 ml of ethyl acetate and washed two times with 20 ml of saturated aqueous sodium chloride solution. The resultant reaction liquid was subjected to a layer separation treatment, the resultant organic layer was distilled under reduced pressure (20 mmHg, 55 to 57° C.), the resultant residue was refined by a chromatography on silica gel using an eluting solvent:hexane/ethyl acetate mixture in a mixing ratio by volume of 10/1. As a colorless liquid fraction, the target 1-acetoxy-2-methyl-3-(2,5-dimethoxyphenyl)propene was obtained in a yield of 77.4% in an amount of 1.94 g in the form of a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07173148B2
出典データセットuspto-grants-2007_02
ORD IDord-c6025d56d0444595a1677ec7688d7cfa
出典メモuspto-grants-2007_02