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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37015Erstellt: 25. Oktober 2026

Dimethylformamide → 3-Acetylthio-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine

https://huagongshe.com/reaction/37015

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktSodium hydrideHCID 24758—
Edukt3-Methanesulphonyloxy-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidineHCID 53997171—
EduktHCID 178418634HCID 178418634—
LösungsmittelWaterHCID 962—
Produkt3-Acetylthio-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidineHCID 5403714579,1%

Reaktionsschritte

To 300 ml of anhydrous N,N-dimethylformamide were added 7.35 g of sodium hydride in the form of a 55% w/w/ dispersion in oil, followed by 12.5 g of thioacetic acid. The mixture was then stirred for 10 minutes, with ice-cooling, after which 40 g of 3-methanesulphonyloxy-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine were added. The mixture was then stirred for 3 hours at 65° C. After the reaction mixture had been allowed to cool, water was added and the mixture was extracted with ethyl acetate. The extract was washed with water and dried and then the solvent was distilled off under reduced pressure. The residue was purified by chromatography through a column of silica gel, eluted with a 2:1 by volume mixture of benzene and ethyl acetate, to give 30 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE034960
Quelldatensatzuspto-grants-1995_05
ORD IDord-10b960678bc34a7c81eff1c395c66e14
Quellennotizuspto-grants-1995_05