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HRID 231227作成日:2026年10月25日

Sulfuric Acid → cis-4-Acetyl-3-[1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone

https://huagongshe.com/reaction/231227

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Sodium BicarbonateHCID 516892—
反応物Water ethylacetateHCID 22728543—
反応物Cis-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-trimethylsilylethynyl-2-azetidinoneHCID 57192380—
触媒Mercuric sulfateHCID 24544—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物cis-4-Acetyl-3-[1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinoneHCID 6778942918.1%

反応手順

Cis-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-trimethylsilylethynyl-2-azetidinone (0.24 g) is dissolved in a mixture of tetrahydrofuran (5 ml) and water (1 ml), and mercury sulfate (0.03 g) and concentrated sulfuric acid (0.06 g) are added, followed by stirring at room temperature for 15 hours. After addition of sodium hydrogen carbonate (0.2 g), the reaction mixture is poured into ethyl acetate-water, and the organic layer is separated, washed with aqueous sodium chloride, dried over magnesium sulfate and concentrated under reduced pressure. The residue is subjected to silica gel column chromatography to give 0.03 g of cis-4-acetyl-3-[1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04845210
出典データセットuspto-grants-1989_07
ORD IDord-cc66650d54a44bf4858200e34e1686f6
出典メモuspto-grants-1989_07