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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1679570Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1679570

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-chloro-N-methyl-p-toluenesulfonamideHCID 13017215—
Eduktp-Nitrobenzyl 6-phenoxyacetamido-2,2-dimethylpenam-3-carboxylate-1-oxideHCID 67928276—
Produktp-Nitrobenzyl 3-Methyl-2-(2-chlorosulfinyl-4-oxo-3-phenoxyacetamido-1-azetidinyl)-3-butenoateHCID 9936995—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04081440
Quelldatensatzuspto-grants-1978_03
ORD IDord-1006accfc76e47c697b583e953dc30c6
Quellennotizuspto-grants-1978_03