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HRID 1710237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/1710237

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

714 mg of 2-ethoxy-2-hydroxyacetic acid p-nitrobenzyl ester and 4 g of molecular sieve A4 are added to a solution of 245 mg of (3S,4R)-4-acetylthio-3-methoxy-2-oxoazetidine in a mixture of 8 ml of toluene and 2 ml of dimethylformamide and the mixture is stirred overnight at room temperature. The molecular sieves are filtered off from the mixture and the filtrate is concentrated by evaporation in vacuo. The residue is chromatographed over silica gel, and by elution with toluene/ethyl acetate (9:1 and 4:1) the title compound, contaminated with some glyoxylate, is obtained.

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-a4e360f1257f4fb4867c6c83b38cf7fd
出典メモuspto-grants-1990_08