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HRID 26686作成日:2026年10月25日

Barium Sulfate → Methyl 2-[2,3-dihydro-2-ethyl-3-methyl-4-oxo-4H-1-benzopyran-6-yl]propionate

https://huagongshe.com/reaction/26686

反応式

関与物質

役割名称HCID仕込み量
反応物Barium SulfateHCID 24414—
反応物Methyl 2-[2-ethyl-3-methyl-4-oxo-4H-1-benzopyran-6-yl]propionateHCID 21322008—
反応物Jones' reagentHCID 131709961—
触媒PalladiumHCID 23938—
溶媒AcetoneHCID 180—
溶媒EthanolHCID 702—
生成物Methyl 2-[2,3-dihydro-2-ethyl-3-methyl-4-oxo-4H-1-benzopyran-6-yl]propionateHCID 21322013—

反応手順

Methyl 2-[2-ethyl-3-methyl-4-oxo-4H-1-benzopyran-6-yl]propionate (6.61 g) was taken up in dry ethanol (150 ml) and hydrogenated at 85 p.s.i. with 5% palladium on carbon (0.2 g) and 5% palladium on barium sulphate (0.49) for a total of 48 hours. The catalyst was removed by filtration (`Hyflo` supercel) and the ethanol removed in vacuo affording an oil. The oil was taken up in acetone (50 ml) and treated with a slight excess of Jones reagent. The excess oxidant was destroyed with methanol and the reaction mixture was dissolved in water (200 ml) and extracted with ether. The combined ethereal extracts were washed with water, dilute aqueous sodium bicarbonate solution and water, dried (MgSO4) and concentrated in vacuo to give the title compound as an oil--6 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04151179
出典データセットuspto-grants-1979_04
ORD IDord-15c03e503fec4509a2e2f164f7947f2d
出典メモuspto-grants-1979_04