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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2091412생성일: 2026년 10월 25일

Water → 2-methyl-1-[3-methyl-5-(tetrahydro-2H-thiopyran-4-yloxy)-1-benzofuran-2-yl]propan-1-one

https://huagongshe.com/reaction/2091412

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Tetrahydro-2h-thiopyran-4-yl 4-methylbenzenesulfonateHCID 270400—
반응물1-(5-Hydroxy-3-methyl-1-benzofuran-2-yl)-2-methylpropan-1-oneHCID 66778555—
용매DimethylformamideHCID 6228—
생성물2-methyl-1-[3-methyl-5-(tetrahydro-2H-thiopyran-4-yloxy)-1-benzofuran-2-yl]propan-1-oneHCID 6677781161%

반응 조건

온도80 °C

반응 단계

A solution of 1-(5-hydroxy-3-methyl-1-benzofuran-2-yl)-2-methylpropan-1-one (1.0 g) synthesized above, tetrahydro-2H-thiopyran-4-yl 4-methylbenzenesulfonate (2.99 g) and tripotassium phosphate (1.26 g) in N,N-dimethylformamide (10 mL) was stirred at 80° C. for 3 hr then at 100° C. for 14 hr. Tetrahydro-2H-thiopyran-4-yl 4-methylbenzenesulfonate (2.99 g) was added to the mixture, and the mixture was stirred at 100° C. for 20 min. Tripotassium phosphate (600 mg) was added to the mixture, and the mixture was stirred at 100° C. for 2 hr then at 120° C. for 3 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated. The residue was subjected to silica gel column chromatography (hexane-ethyl acetate 100:0-90:10, v/v) to give the title compound (886 mg, 61%) as an orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08436043B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-f20c42aa3ee042799097f2c9983bbde5
출처 메모uspto-grants-2013_05