戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1710246作成日:2026年10月27日

2-Ethoxy-2-hydroxyacetic acid p-nitrobenzyl ester → 2-[(3S,4R)-4-acetylthio-3-methoxy-2-oxoazetidin-1-yl]-2-hydroxyacetic acid p-nitrobenzyl ester

https://huagongshe.com/reaction/1710246

反応式

関与物質

役割名称HCID仕込み量
反応物2-Ethoxy-2-hydroxyacetic acid p-nitrobenzyl esterHCID 11043316—
反応物(3S,4R)-4-acetylthio-3-methoxy-2-oxoazetidineHCID 56630779—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物2-[(3S,4R)-4-acetylthio-3-methoxy-2-oxoazetidin-1-yl]-2-hydroxyacetic acid p-nitrobenzyl esterHCID 56607651—

反応手順

1.15 g of 2-ethoxy-2-hydroxyacetic acid p-nitrobenzyl ester and 4 g of molecular sieves A4are added to a solution of 350 mg of (3S,4R)-4-acetylthio-3-methoxy-2-oxoazetidine in a mixture of 24 ml of absolute toluene and 6 ml of absolute dimethylformamide and the mixture is stirred overnight at room temperature under nitrogen. The molecular sieves are filtered off and the filtrate is concentrated by evaporation in vacuo. The residue is chromatographed over silica gel, and the title compound is obtained by eluting with toluene and toluene/ethyl acetate (19:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04952690
出典データセットuspto-grants-1990_08
ORD IDord-238988504a214b94aa1f9eb38d617296
出典メモuspto-grants-1990_08