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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Potassium Phosphate, Tribasic | HCID 62657 | — |
| 반응물 | Tetrahydro-2h-thiopyran-4-yl 4-methylbenzenesulfonate | HCID 270400 | — |
| 반응물 | 1-(5-Hydroxy-3-methyl-1-benzofuran-2-yl)-2-methylpropan-1-one | HCID 66778555 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-methyl-1-[3-methyl-5-(tetrahydro-2H-thiopyran-4-yloxy)-1-benzofuran-2-yl]propan-1-one | HCID 66777811 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08436043B2 |
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| 출처 데이터셋 | uspto-grants-2013_05 |
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| ORD ID | ord-f20c42aa3ee042799097f2c9983bbde5 |
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| 출처 메모 | uspto-grants-2013_05 |
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