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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 441053생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/441053

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Carbon DisulfideHCID 6348—
반응물18-Crown-6HCID 28557—
반응물Potassium hydrideHCID 82127—
반응물1-[2-Hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanoneHCID 10879697—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물5,7-Bis(methoxymethoxy)-2-methylthiochromoneHCID 5708550791.6%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05521216
출처 데이터셋uspto-grants-1996_05
ORD IDord-81be17509c404bde932adfb2225d6ac0
출처 메모uspto-grants-1996_05