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HRID 2406408作成日:2026年10月27日

4H-pyran-4-one → 4-Methylbenzaldehyde

https://huagongshe.com/reaction/2406408

反応式

関与物質

役割名称HCID仕込み量
反応物4H-pyran-4-oneHCID 7968—
反応物MorpholineHCID 8083—
反応物3-(4-Methylphenyl)-3-oxopropanenitrileHCID 522513—
反応物SulfurHCID 5362487—
溶媒EthanolHCID 702—
生成物4-MethylbenzaldehydeHCID 772576.9%

反応条件

温度40 °C

反応手順

4-Pyranone (2.31 mL, 24.97 mmol) and sulphur (801 mg, 24.97 mmol) were added to a solution of 3-oxo-3-p-tolyl-propionitrile (3.79 g, 23.8 mmol) in ethanol (40 mL) followed by morpholine (2.18 mL, 24.97 mmol) and the reaction heated at 40° C. for 16 hours, The reaction mixture was concentrated in vacuo and the residue purified by flash chromatography on silica eluting with 0-20% ethylacetate/heptanes to afford 12-Amino-4,7-dihydro-5H-thieno[2,3-c]pyran-3-yl)-p-tolyl-methanone as a yellow solid (2.2 g, 36% yield). LCMS (2 min acidic) 1.07 min ES+/AP+ 274 (MH+). 1HNMR (400 MHz, CDCl3) δ ppm 2.00-2.03 (m, 2H), 2.42 (s, 3H), 3.80-3.84 (m, 2H), 4.80 (s, 2H), 6.60 (br s, 2H), 7.20 (d, 2H), 7.41 (d, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08809363B2
出典データセットuspto-grants-2014_08
ORD IDord-137b9c2d900f476f9a9343f506ac1196
出典メモuspto-grants-2014_08