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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1900714생성일: 2026년 10월 27일

Ethanol → 2-Methanesulfonyloxymethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one

https://huagongshe.com/reaction/1900714

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물PyridineHCID 1049—
반응물Methanesulfonyl chlorideHCID 31297—
반응물2-Hydroxymethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-oneHCID 23369679—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
생성물2-Methanesulfonyloxymethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-oneHCID 23369644—

반응 단계

2-Hydroxymethyl-5-methyl-2,3,6,7-tetrahydrofuro[2,3-f]quinoline-7-one (1.2 g) was added to anhydrous pyridine (24 ml). The mixture was stirred on ice, during which methanesulfonylchloride (625 mg) was added thereto, followed by stirring at room temperature for 100 minutes. Methanesulfonylchloride (283 mg) was added again and stirred at the same temperature for 50 minutes. After completion of the reaction, a small amount of ethanol was added, and the mixture was brought to dryness under reduced pressure. The residue was dissolved in a solvent mixture of chloroform and methanol (10:1), washed with diluted HCl, sodium bicarbonate water, and aqueous NaCl solution in this order, and dried. When the solvent was evaporated, 1.6 g (quantitative assay) of the title compound was obtained. This substance was recrystallized from a solvent mixture of chloroform-n-hexane, obtaining colorless powdery crystals having a melting point of 200°-203° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05576324
출처 데이터셋uspto-grants-1996_11
ORD IDord-9e9d94a0bfea42afa73dedfc4b5b02f5
출처 메모uspto-grants-1996_11