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HRID 620791作成日:2026年10月25日

Water → HCID 54162700、化合物

https://huagongshe.com/reaction/620791

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl bromoacetateHCID 7748—
反応物tert-butyl (2S,4R)-4-((tert-butyldimethylsilyl)oxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 11078078—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 54162700HCID 54162700—

反応手順

To a solution of (2S,4R)-1-t-butoxycarbonyl-4-t-butyldimethylsilyloxy-2-hydroxymethylpyrrolidine (1.00 g) in tetrahydrofuran (20 ml) was dropwise added a 1.6 M solution of butyllithium in hexane (2 ml) at -40°~-30° C. in a nitrogen stream and the mixture was stirred at the same temperature for 30 minutes. To the reaction mixture was added ethyl bromoacetate (0.40 ml) at -40°~-30° C. and the reaction mixture was stirred at -40°~-30° C. for 30 minutes and then at ambient temperature for 3 hours. The mixture was poured into a mixture of water (50 ml) and ethyl acetate (50 ml). The organic layer was washed with brine (50 ml), dried over magnesium sulfate and concentrated under reduced pressure to give a syrup. The syrup was subjected to a column chromatography on silica gel (20 g) and eluted with chloroform to give (2S,4R)-1-t-butoxycarbonyl-4-t-butyldimethylsilyloxy-2-(ethoxycarbonylmethyloxymethyl)pyrrolidine (0.88 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04822787
出典データセットuspto-grants-1989_04
ORD IDord-a35f83cd45634c3b95b15101fef6f8ba
出典メモuspto-grants-1989_04