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HRID 260716作成日:2026年10月27日

3-Methylcatechol → 5-Methyl-1,4-benzodioxane

https://huagongshe.com/reaction/260716

反応式

関与物質

役割名称HCID仕込み量
反応物3-MethylcatecholHCID 340—
反応物1,2-DibromoethaneHCID 7839—
反応物Potassium CarbonateHCID 11430—
溶媒DimethylformamideHCID 6228—
生成物5-Methyl-1,4-benzodioxaneHCID 1223882782%

反応条件

温度125 °C

反応手順

In 300 ml of dry dimethylformamide, was dissolved 30 g of 3-methylcatechol and then 100 g of potassium carbonate was added to the solution. This solution was heated to 120 to 130° C. and 136 g of 1,2-dibromoethane was added dropwise in ten and several portions. After stirring for 30 minutes under the same conditions, the mixture was cooled and solid materials were removed by filtration. To the filtrate, was added diethyl ether, and the mixture was washed successively with a 3% sodium hydroxide aqueous solution, water and saturated saline solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The resulting oily material was purified by silica gel column chromatography to obtain 29.7 g of the titled 5-methyl-1,4-benzodioxane (yield: 82%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05530021
出典データセットuspto-grants-1996_06
ORD IDord-758c32b988024af7807e7840d85e4998
出典メモuspto-grants-1996_06