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HRID 2259752作成日:2026年10月26日

Dopac → 5-(2-Hydroxyethyl)-2-methyl-1,3-benzodioxole

https://huagongshe.com/reaction/2259752

反応式

関与物質

役割名称HCID仕込み量
反応物DopacHCID 547—
反応物Vinyl AcetateHCID 7904—
反応物Sodium HydroxideHCID 14798—
反応物Aluminium lithium hydrideHCID 21226445—
触媒Mercuric oxideHCID 30856—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物5-(2-Hydroxyethyl)-2-methyl-1,3-benzodioxoleHCID 1900162574.6%

反応手順

A suspension of 1.0 g of 3,4-dihydroxyphenylacetic acid, 1.4 g of vinyl acetate, 6 mg of mercury oxide (yellow) and 0.03 ml of boron fluoride/ethyl etherate in 9 ml of toluene was stirred at room temperature for 14 h. The reaction mixture was diluted with ethyl acetate and washed with water and an aqueous common salt solution. The organic layer was dried over magnesium sulfate and the solvent was distilled off. An oil thus obtained was dissolved in 10 ml of tetrahydrofuran and the solution was added dropwise to a suspension of 0.5 g of lithium aluminum hydride in tetrahydrofuran under cooling with ice. The mixture was stirred at room temperature for 1 h. 0.5 ml of water, then 0.5 ml of a 15% aqueous sodium hydroxide solution and finally 1.5 ml of water were added thereto and an insoluble matter was filtered off. The filtrate was concentrated and treated according to silica gel column chromatography (ethyl acetate/hexane=1:1) to obtain 0.8 g of the intended compound in the form of a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05475024
出典データセットuspto-grants-1995_12
ORD IDord-237408a16d374957be2a2740e478e8d8
出典メモuspto-grants-1995_12