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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261313생성일: 2026년 10월 24일

N-chloro-N-methyl-p-toluenesulfonamide → p-Nitrobenzyl 3-Methyl-2-(2-chlorosulfinyl-4-oxo-3-phenoxyacetamido-1-azetidinyl)-3-butenoate

https://huagongshe.com/ko/reaction/261313

반응식

참여 물질

역할이름HCID투입량
반응물N-chloro-N-methyl-p-toluenesulfonamideHCID 13017215—
반응물p-Nitrobenzyl 6-phenoxyacetamido-2,2-dimethylpenam-3-carboxylate-1-oxideHCID 67928276—
생성물p-Nitrobenzyl 3-Methyl-2-(2-chlorosulfinyl-4-oxo-3-phenoxyacetamido-1-azetidinyl)-3-butenoateHCID 9936995—

반응 단계

To 150 ml. of distilled and molecular sieve-dried toluene were added 3.0 g. (6 mmol.) of p-nitrobenzyl 6-phenoxyacetamido-2,2-dimethylpenam-3-carboxylate-1-oxide and 1.3 g. (6 mmol.) of N-chloro-N-methyl-p-toluenesulfonamide. The mixture was heated at reflux for 60 minutes. The resulting reaction mixture then was cooled to room temperature. An aliquot (15 ml.) was separated, washed with water, and brine, dried over magnesium sulfate, and evaporated to dryness in vacuo. The nmr spectrum of the residue was consistent for the title compound contaminated with some N-methyl-p-toluenesulfonamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04165315
출처 데이터셋uspto-grants-1979_08
ORD IDord-a641228144254f99a5c289426dabe60c
출처 메모uspto-grants-1979_08