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HRID 231239作成日:2026年10月24日

Sulfuric Acid → HCID 13277552、化合物

https://huagongshe.com/ja/reaction/231239

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TetrahydrofuranHCID 8028—
反応物Sodium BicarbonateHCID 516892—
反応物(3S,4S)-3-[(R)-1-hydroxyethyl]-4-trimethylsilylethynyl-2-azetidinoneHCID 53965319—
触媒Mercuric sulfateHCID 24544—
溶媒WaterHCID 962—
生成物HCID 13277552HCID 13277552—

反応条件

温度25 °C

反応手順

trans i.e. (3S,4S)-3-[(R)-1-hydroxyethyl]-4-trimethylsilylethynyl-2-azetidinone (0.08 g) is dissolved in a mixture of tetrahydrofuran (10 ml) and water (2 ml), and 0.02 g of mercury sulfate and a catalytic amount of concentrated sulfuric acid are added, followed by stirring at 25° C. for 3 hours. After addition of 0.1 g of sodium hydrogen carbonate, the mixture is concentrated to dryness under reduced pressure. The residue is extracted with 50 ml of ethyl acetate and the extract is concentrated to dryness. The residue is dissolved in 10 ml of ethyl acetate, and m-chloroperbenzoic acid (0.2 g) is added, followed by strirring for 50 hours. After addition of 0.2 ml of dimethyl sulfide, and the mixture is stirred further for 30 minutes and concentrated under reduced pressure. The residue is subjected to silica gel column chromatography (eluent: 60% ethyl acetate-40% n-hexane) to give trans i.e. (3S,4R)-4-acetoxy-3-[(R)-1-hydroxyethyl]-2-azetidinone (0.04 g).

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-14d9b31fc918400fa4ea5c428c04bca9
出典メモuspto-grants-1989_07