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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5357생성일: 2026년 10월 23일

Methyl iodide → 3-Ethoxycarbonyl-2-methylthio-4-oxo-6,7,8-trifluoro-4H-1-benzothiopyran

https://huagongshe.com/ko/reaction/5357

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Carbon DisulfideHCID 6348—
반응물TriethylamineHCID 8471—
반응물Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 600916—
용매Dimethyl SulfoxideHCID 679—
생성물3-Ethoxycarbonyl-2-methylthio-4-oxo-6,7,8-trifluoro-4H-1-benzothiopyranHCID 2177022274%

반응 단계

To a solution of 3.00 g (11.4 mmol) of ethyl 2,3,4,5-tetrafluorobenzoylacetate, 870 mg (11.4 mmol) of carbon disulfide and 9 ml of dried dimethyl sulfoxide were added 2.31 g (22.8 mmol) of triethylamine at room temperature, and the mixture was stirred for 1 hour at room temperature. Then, at room temperature, 3.24 g (22.8 mmol) of methyl iodide were added and the mixture was stirred for 2 hours, which was poured into ice-water. The crystals deposited were collected by filtration and dried to obtain 2.81 g (8.41 mmol) of title compound (yield 74%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244892
출처 데이터셋uspto-grants-1993_09
ORD IDord-93c2e2181a674049914d3893aea5bed6
출처 메모uspto-grants-1993_09