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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127458생성일: 2026년 10월 25일

Ozone → 2-[4-(Benzoxazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-hydroxy-crotonic acid diphenylmethyl ester

https://huagongshe.com/reaction/127458

반응식

참여 물질

역할이름HCID투입량
반응물OzoneHCID 24823—
반응물Toluene ethylacetateHCID 21584019—
반응물2-[4-(Benzoxazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methylene-butyric acid diphenylmethyl esterHCID 53800147—
반응물Oxygen ozoneHCID 131711318—
용매Ethyl AcetateHCID 8857—
생성물2-[4-(Benzoxazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-hydroxy-crotonic acid diphenylmethyl esterHCID 86736447—

반응 단계

(aix) Approximately one equivalent of ozone (in the form of an O2 /O3 mixture) is passed into a solution, cooled to -70° C., of 3.35 g of 2-[4-(benzoxazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methylene-butyric acid diphenylmethyl ester in 125 ml of ethyl acetate, until starting material is no longer detectable by thin layer chromatography (silica gel; toluene/ethyl acetate, 3:1). The solution is concentrated by evaporation to about 50 ml in vacuo, mixed with 5 ml of dimethyl sulphide and stirred until the potassium iodide/starch test no longer gives a reaction. The mixture is concentrated by evaporation in vacuo, the residue is dissolved in 150 ml of benzene and the solution is washed with water. The organic phase is dried over sodium sulphate and concentrated by evaporation. The residue is chromatographed on 150 g of acid-washed silica gel, using toluene/ethyl acetate, 4:1. 2-[4-(Benzoxazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-hydroxy-crotonic acid diphenylmethyl ester is obtained in the form of a white foam; IR spectrum (methylene chloride): characteristic bands at 5.60, 5.90 and 6.0μ.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04255328
출처 데이터셋uspto-grants-1981_03
ORD IDord-de20d7449bb049aa8a8941f1cae6cff4
출처 메모uspto-grants-1981_03