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HRID 374482作成日:2026年10月26日

4-Hydroxybenzaldehyde → (R)-(-)-4-(oxiranylmethoxy)-benzaldehyde

https://huagongshe.com/reaction/374482

反応式

関与物質

役割名称HCID仕込み量
反応物4-HydroxybenzaldehydeHCID 126—
反応物Potassium CarbonateHCID 11430—
反応物Benzenesulfonic acid, 3-nitro-, (2R)-2-oxiranylmethyl esterHCID 146513—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物(R)-(-)-4-(oxiranylmethoxy)-benzaldehydeHCID 703749889.1%

反応手順

In 800 ml of anhydrous methyl ethyl ketone was dissolved 23.54 g of 4-hydroxybenzaldehyde and 50 g of (R)-(-)-glycidyl m-nitrobenzenesulfonate. To the solution was added 34.6 g of anhydrous potassium carbonate, and the mixture was refluxed with heating for 2.5 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was extracted with ethyl acetate. The extract was washed with water, dried with magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified with chloroform to give 30.6 g of the title compound (yield 89%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05480899
出典データセットuspto-grants-1996_01
ORD IDord-0142865354294b02b38cff5746f2279e
出典メモuspto-grants-1996_01