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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1679572생성일: 2026년 10월 27일

Water → p-Nitrobenzyl 3-Methyl-2-(2-chlorosulfinyl-4-oxo-3-phenoxyacetamido-1-azetidinyl)-3-butenoate

https://huagongshe.com/reaction/1679572

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물N-ChlorophthalimideHCID 18997—
반응물p-Nitrobenzyl 6-phenoxyacetamido-2,2-dimethylpenam-3-carboxylate-1-oxideHCID 67928276—
용매TolueneHCID 1140—
생성물p-Nitrobenzyl 3-Methyl-2-(2-chlorosulfinyl-4-oxo-3-phenoxyacetamido-1-azetidinyl)-3-butenoateHCID 9936995—

반응 단계

Toluene (425 ml.) was heated in equipment containing a Dean-Stark water trap to azeotropically remove any moisture which may be present, and 25 ml. of toluene were removed thereby. To the remaining toluene were added 10.0 g. (20 mmol.) of p-nitrobenzyl 6-phenoxyacetamido-2,2-dimethylpenam-3-carboxylate-1-oxide, the toluene being maintained at a temperature slightly below reflux. Toluene (200 ml.) was separately distilled, and 4.0 g. (22 mmol.) of N-chlorophthalimide were added. The resulting solution (warm) was added dropwise to the solution of the penicillin sulfoxide ester over a period of 30 minutes. The mixture remained a light yellow solution throughout addition. The mixture then was refluxed for 55 minutes after which time a sample was removed, and nmr (CDCl3) analysis of the sample indicated virtually entire conversion of the penicillin sulfoxide ester to the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04081440
출처 데이터셋uspto-grants-1978_03
ORD IDord-9ac5dc081e674a428cea35f2b0a87473
출처 메모uspto-grants-1978_03