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HRID 426457作成日:2026年10月26日

Oxygen → 4-Acetylthio-2-azetidinone

https://huagongshe.com/reaction/426457

反応式

関与物質

役割名称HCID仕込み量
反応物OxygenHCID 977—
反応物4-Acetoxy-2-azetidinoneHCID 119981—
反応物HCID 178418361HCID 178418361—
反応物HCID 178418634HCID 178418634—
生成物4-Acetylthio-2-azetidinoneHCID 1313205891%

反応手順

To a cold (0°-5° C.) oxygen-free 1 N NaOH solution (27.5 ml.) was added thioacetic acid (2.09 g., 27.5 mmole) at such a rate that the temperature was maintained between 0°-5° C. The resulting solution was added dropwise (over 20 min.) to a cold (0.5° C.) oxygen-free aqueous solution (11 ml.) of 4-acetoxy-2-azetidinone (3.23 g., 25 mmole) [prepared in Liebigs Ann. Chem., 539 (1974)]. The reaction mixture was stirred under a nitrogen atmosphere for 0.5 hr. at 0°-5° C. and for 2-2.5 hr. at 23°-25° C. before being extracted with chloroform (4×25 ml.). The organic extracts were combined, washed with water (10 ml.), dried over anhydrous Na2SO4 and concentrated to a yellow syrup, 3.3 g., 91% yield. The title product was found to be identical to the sample prepared by Clauss in Liebigs Ann. Chem., 539 (1974). δ (ppm, CDCl3), 7.2 (1H, NH), 5.23 (1H, dd, Jcis =2.8, Jtrans =5.0, H-H), 3.55 (1H, ddd, Jgem =15.2, JHNH =2.0, H-3 trans), 2.95 (1H, ddd, Jgem =15.2, Jcis =2.8, JHNHSl, H-3 cis) and 2.36 (3H, s, methyl).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04169833
出典データセットuspto-grants-1979_10
ORD IDord-b3cb39ef36fb4233ad29b0fa1272c1bd
出典メモuspto-grants-1979_10