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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52007생성일: 2026년 10월 23일

Dimedone → 5-(4,6-Dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylic Acid

https://huagongshe.com/ko/reaction/52007

반응식

참여 물질

역할이름HCID투입량
반응물DimedoneHCID 31358—
반응물Allyl 5-(4,6-dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylateHCID 53832981—
용매TetrahydrofuranHCID 8028—
생성물5-(4,6-Dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylic AcidHCID 5446801991.4%

반응 단계

1.60 g of allyl 5-(4,6-dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylate and 0.54 g of dimedone were dissolved in 14 ml of tetrahydrofuran, and 40 mg of tetrakistriphenylphosphine palladium (0) was added thereto under a nitrogen atmosphere. The mixture was stirred at room temperature for 3 hours. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=2/1) to obtain 1.33 g (yield: 91%) of the desired compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616537
출처 데이터셋uspto-grants-1997_04
ORD IDord-20301908661145a2bcc9f8c17eecf4a7
출처 메모uspto-grants-1997_04