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HRID 9667作成日:2026年10月25日

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

https://huagongshe.com/reaction/9667

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物Phosphorus oxide (P4O10)HCID 14812—
反応物4-Methoxy-3-methylphenylacetic acidHCID 138276—
反応物Sodium BicarbonateHCID 516892—
反応物Thiophene, 4-methyl-2-[4-(trifluoromethyl)phenyl]-HCID 21986373—
溶媒WaterHCID 962—
生成物2-(4-Methoxy-3-methylphenyl)-1-{3-methyl-5-[4-(trifluoromethyl)phenyl]thien-2-yl}ethanoneHCID 21986370—

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091237B2
出典データセットuspto-grants-2006_08
ORD IDord-450d571946b54fa997b752c94963e482
出典メモuspto-grants-2006_08