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HRID 441053作成日:2026年10月27日

Methyl iodide → 5,7-Bis(methoxymethoxy)-2-methylthiochromone

https://huagongshe.com/reaction/441053

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Carbon DisulfideHCID 6348—
反応物18-Crown-6HCID 28557—
反応物Potassium hydrideHCID 82127—
反応物1-[2-Hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanoneHCID 10879697—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5,7-Bis(methoxymethoxy)-2-methylthiochromoneHCID 5708550791.6%

反応手順

Under cooling on ice, potassium hydride (0.5 ml of 35% mineral oil) was suspended in 2 ml THF. 2 ml of 126 mg of 2'-hydroxy-4',6'-bis(methoxymethoxy)acetophenone (0.492 mmol) and 130 mg of 18-crown-6 (0.492 mmol) in THF was added dropwise to the above suspension, and the mixture was stirred for 1 hour. After addition of 0.89 ml of carbon disulfide (14.76 mmol), the solution was stirred for 20 hours at room temperature. Then, 0.5 ml of methyl iodide was added thereto, and the solution was stirred for 30 min. After water was slowly added thereto, the reaction solution was extracted twice with ether, and the organic layer was washed with saturated NaCl water and then dried over sodium sulfate anhydride. The solvent was distilled off and the resulting crude product was washed with hexane, to give 133.5 mg of 5,7-bis(methoxymethoxy)-2-methylthiochromone (87% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05521216
出典データセットuspto-grants-1996_05
ORD IDord-81be17509c404bde932adfb2225d6ac0
出典メモuspto-grants-1996_05