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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1108077생성일: 2026년 10월 25일

Methyl 4-(3-mercaptophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate → Ethyl 4-[3-[4-(2-methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate

https://huagongshe.com/reaction/1108077

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 4-(3-mercaptophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylateHCID 11242202—
반응물1-(4-iodophenyl)-2-methyl-1H-imidazoleHCID 11289090—
반응물Sodium t-butoxideHCID 23676156—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
생성물Ethyl 4-[3-[4-(2-methylimidazol-1-yl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxylateHCID 1115443160.9%

반응 단계

A solution of methyl 4-(3-mercaptophenyl)-3,4,5,6-tetrahydro-2H-pyran-4-carboxylate (1.04 g, 3.5 mmol), 4-(2-methylimidazol-1-yl)phenyliodide (0.89 g, 3.5 mmol), sodium t-butoxide (673 mg, 7 mmol) and tetrakis(triphenylphosphine)palladium (162 mg, 0.14 mmol) in dry ethanol (20 ml) was heated to reflux with stirring overnight. Volatiles were remeved by evaporation and the residue was partitioned between ethyl acetate (100 ml) and water (100 ml). The aqueous layer was extracted with ethyl acetate (100 ml). The combined organic layers were washed with brine (100 ml), dried (magnesium sulfat) and concentrated to dryness to give 1.09 g of crude product as a brown liquid. Purification by column chromatography (silica-gel, 50 g; methanol in dichloromethane, increasing the ratio of methanol from 0% to 4%) afforded the titled compound (0.90 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06063928
출처 데이터셋uspto-grants-2000_05
ORD IDord-c8111a64e6d54f2191828c98f2bea4d2
출처 메모uspto-grants-2000_05