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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9667생성일: 2026년 10월 24일

Methanesulfonic Acid → 2-(4-Methoxy-3-methylphenyl)-1-{3-methyl-5-[4-(trifluoromethyl)phenyl]thien-2-yl}ethanone

https://huagongshe.com/ko/reaction/9667

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물4-Methoxy-3-methylphenylacetic acidHCID 138276—
반응물Sodium BicarbonateHCID 516892—
반응물Thiophene, 4-methyl-2-[4-(trifluoromethyl)phenyl]-HCID 21986373—
용매WaterHCID 962—
생성물2-(4-Methoxy-3-methylphenyl)-1-{3-methyl-5-[4-(trifluoromethyl)phenyl]thien-2-yl}ethanoneHCID 21986370—

반응 조건

온도60 °C

반응 단계

To methanesulfonic acid (8 ml) in a flask under N2 was added P2O5 (0.56 g), the resulting suspension was heated to 60° C. until a clear solution formed. The mixture was cooled to room temperature prior to addition of 4-methoxy-3-methyl-phenylacetic acid (0.3549) and 4-methyl-2-[4-(trifluoromethyl)phenyl]thiophene (intermediate 102, 0.4 g). The mixture was then heated to 60° C. for 90 minutes. The reaction mixture was cooled to room temperature and then poured into iced water. The suspension was made basic by cautious addition of NaHCO3 and the products extracted into ethyl acetate. The combined organic extracts were dried (MgSO4), filtered and evaporated to yield a brown oil. Purification by flash column chromatography eluting with 5% EtOAc/cyclohexane yielded the title compound as a brown gum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091237B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-450d571946b54fa997b752c94963e482
출처 메모uspto-grants-2006_08